A pyrazole derivative of the formula I ##STR1## wherein A is c1 -c4 alkyl, c2 -c4 alkenyl or c2 -c4 alkynyl; B is hydrogen, c1 -c3 alkyl, halogen, c1 -c3 haloalkyl, c1 -c3 alkoxy, c1 -c3 alkylthio, c2 -c4 alkoxyalkyl, c2 -c4 alkylthioalkyl or c2 -c4 alkoxycarbonyl; X is c1 -c6 alkyl, c1 -c6 alkoxy, halogen, nitro, cyano, etc.; Y is --OR1 (wherein R1 is c3 -c8 cycloalkyl, etc), --O--L--O--R1 (wherein L is c1 -c6 alkylene which may be substituted by c1 -c3 alkyl), --O--L--OH, --O--L--O--L--O--R2 (wherein R2 is hydrogen, c1 -c6 alkyl group, etc.), --O--L--R3 (wherein R3 is phenyl which may be substituted by c1 -c3 alkyl, etc.), --O--M (wherein M is a 3- to 6-membered alicyclic group), --O--L--M, --O--L--NR4 R5 (wherein each of R4 and R5 is hydrogen or c1 -c6 alkyl, or R4 and R5 form a ring together with the adjacent nitrogen atom), --O--L--COOR4, --O--CH═CH--COOR4, --O--L--CN, --O--L--c(O)--R2, --O--L--S(O)n --R4 (wherein n is an integer of from 0 to 2), --O--COOR4, --O--CONR4 R5, --OP(O)(OR4)2, --S(O)n R1, or --S(O)n --L--O--R1 ; Z is halogen, nitro, c1 -c3 alkoxy, etc.; V is hydrogen, halogen, c1 -c4 alkyl or c1 -c4 alkoxy; W is hydrogen, halogen, c1 -c4 alkyl, etc.; Q is hydrogen, c1 -c6 alkyl which may be substituted by halogen, . . . --c(O)--R7 (wherein R7 is phenyl which may be substituted), --S(O)2 R7, --P(O)(OR7)2, --L--c(O)--R7, --L--c(O)--N(R8)(R9) (wherein each of R8 and R9 is hydrogenor c1 -c6 alkyl), --L--R10 (wherein R10 is phenyl group may be substituted, c1 -c6 alkyl, c1 -c7 alkoxy, or hydroxyl), --L--N(R8)(R9), --L--OR11 (wherein R11 is hydrogen, c1 -c6 alkyl, or c1 -c6 alkenyl), --L--OC(O)R12 (wherein R12 is c1 -c6 alkyl or c1 -c6 alkoxy), --L--S(O)n R11, --L--SC(O)R8, ##STR2## (wherein each of L1 and L2 is methylene, oxygen or sulfur, R12 is hydrogen or c1 -c3 alkyl, and m is 2 or 3); and a salt thereof.

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Patent
   RE34779
Priority
Jul 15 1988
Filed
Sep 18 1992
Issued
Nov 08 1994
Expiry
Sep 18 2012
Inventors
Suzuki, Ko…
Assg.orig
Nissan Che…
Assg.curr
Nissan Che…
Entity
Large
Referenced by
17
References
10
Maint.:
all paid
EXAMPLE 1
(1) (2-methoxy)ethyl…
(2) 2 -chloro-4-meth…
EXAMPLE 2
(2) 3-benzyloxy-2-ch…
(3)-4-(3-benzyloxy-2…
FORMULATION EXAMPLE 1
FORMULATION EXAMPLE 2
FORMULATION EXAMPLE 3
FORMULATION EXAMPLE 4
FORMULATION EXAMPLE 5
FORMULATION EXAMPLE 6
FORMULATION EXAMPLE 7
TEST EXAMPLE 1:
Standard ratings
TEST EXAMPLE 2:
TEST EXAMPLE 3
7. A pyrazole derivative of the formula I ##STR59## A is a c1 -c4 - alkyl group, a c2 -c4 -alkenyl group, or a c2 -c4 alkynyl group;
B is a hydrogen, a c1 -c3 alkyl group, a halogen atom, a c1 -c3 -haloalkyl group, a c1 -c3 -alkoxy group, a c1 -c3 -alkylthio group, a c2 -c4 -alkoxyalkyl group, a c2 -c4 -alkylthioalkyl group or c2 -c4 -alkoxycarbonyl group;
X is a c1 -c6 -alkyl group, a c1 -c6 -alkoxy group, a halogen atom, a nitro group, a cyano group, a c1 -c6 -haloalkyl group, a c2 -c6 -alkoxyalkyl group, a c2 -c6 -alkylcarbonyl group, a c2 -c6 -alkoxycarbonyl group, an aminocarbonyl group substituted independently by hydrogen or by a c1 -c6 -alkyl group, a c1 -c6 -haloalkoxy group, a c1 -c6 -alkylthio group or a c2 -c6 -alkylthioalkyl group;
Y is --OR1 (wherein R1 is a c3 -c8 -cycloalkyl group, c4 -c8 -cycloalkylalkyl group, a c3 -c6 -alkenyl group, a c2 -c6 -alkynyl group, a c3 -c8 -halocycloalkylalkyl group, a c3 -c6 haloalkenyl group, a c2 -c6 haloalkynyl group, or a c2 -c6 nitroalkyl group), --O--L--O--R (wherein L is a c1 -c6 alkylene group which may be substituted by a c1 -c3 alkyl group, and R is a c1 -c4 alkyl group), --O--L--O--R1 (wherein L is a c1 -c6 alkylene group which may be substituted by a c1 -c3 -alkyl group, and R1 is as defined above), --O--L--OH (wherein L is as defined above), O--L--O--L--O--R2 (wherein L is as defined above, and R2 is a hydrogen atom, a c1 -c6 alkyl group or a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--L--R3 (wherein L is as defined above, and R3 is a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--M (wherein M is a 3- to 6-membered alicyclic group containing not more than two sulfur or oxygen atoms and formed by a linkage of from 1 to 4 carbon atoms), O--L--M (wherein L and M are as defined above), O--L--NR4 R5 (wherein L is as defined above and each of R4 and R5 which may be the same or different is a hydrogen atom or a c1 -c6 alkyl group, or R4 and R5 form a 6-membered ring together with the adjacent nitrogen atom), --O--L--COOR4 (wherein L and R4 are as defined above), --O--CH═CH--COOR4 (wherein R4 is as defined above), --O--L--CN (wherein L is as defined above), --O--L--c(O)-R2 (wherein L and R2 are as defined above, and n is an integer of from 0 to 2), --O--COOR4 (wherein R4 are as defined above), --O--CONR4 R5 (wherein R4 and R5 are as defined above, or --OP(O)(OR4)2 (wherein R4 is as defined above);
Z is a halogen atom, a nitro group, a c1 -c3 alkoxy group, a trifluoromethyl group, a trifluoromethoxy group, a cyano group or --S(O)n R6 (wherein n is as defined above, and R6 is a c1 -c3 alkyl group or a c1 -c3 haloalkyl group);
V is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group or a c1 -c4 alkoxy group;
W is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group, a c1 -c4 haloalkyl group, a c1 -c4 alkoxy group, a c2 -c6 alkoxyalkyl group, a c2 -c5 alkoxycarbonyl group, a c1 -c3 haloalkoxy group, a nitro group, a cyano group or --S(O)n --R6 (wherein n and R6 are as defined above) and
O is selected from the group consisting of CH2 NHCH2 CH═CH2, CH2 NMeCH2 CH═CH2, CH2 NHAc, CH2 NHCOEt, CH2 NHCO2 Me, CH2 NHCO2 Et, CH2 NMeCO2 Me, COCH2 Cl, COCHCl2, COCCl3, COCF3, COCH2 OMe, COCH2 OPh, COCH2 CH═CHCH3, CONHMe, CONMe2, CONHEt, CONEt2, CONPr-n2, CON(CH2 CH═CH2)2, CONMePh, ##STR60## CO2 CH2 Ph, SO2 CH2 CH═CH2, SO2 CF3, P(═S) (OMe)2, P(═S) (OEt)2, P(═O)-(OCH2 CH═CH2)2, P(═O)OPHOCH2 CH═CH2 ; and salts thereof.
5. A pyrazole derivative of the formula I ##STR55## wherein A is a c1 -c4 alkyl group, a c2 -c4 alkenyl group or a c2 -c4 alkynyl group;
B is a hydrogen atom, a c1 -c3 alkyl group, a halogen atom, a c1 -c3 haloalkyl group, a c1 -c3 alkoxy group, a c1 -c3 alkylthio group, a c2 -c4 alkoxyalkyl group, a c2 -c4 alkylthioalkyl group or a c2 -c4 alkoxycarbonyl group;
X is a c1 -c6 alkyl group, a c1 -c6 alkoxy group, a halogen atom, a nitro group, a cyano group, a c1 -c6 haloalkyl group, a c2 -c6 alkoxyalkyl group, a c2 -c6 alkylcarbonyl group, a c2 -c6 alkoxycarbonyl group, an aminocarbonyl group substituted independently by hydrogen or by a c1 -c6 alkyl group, a c1 -c6 haloalkoxy group, a c1 -c6 alkylthio group or a c2 -c6 alkylthioalkyl group;
Y is --OR1 (wherein R1 is a c3 -c8 cycloalkyl group, a c4 -c8 cycloalkylalkyl group, a c3 -c6 alkenyl group, a c2 -c6 alkynyl group, a c1 -c6 haloalkyl group, a c3 -c8 halocycloalkylalkyl group, a c3 -c6 haloalkenyl group, a c2 -c6 haloalkynyl group, a c2 -c6 nitroalkyl group or a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--L--O--R1 (wherein L is a c1 -c6 alkylene group which may be substituted by a c1 -c3 alkyl group, and R1 is as defined above), --O--L--OH (wherein L is as defined above), --O--L--O--L--O--R2 (wherein L is as defined above, and R2 is a hydrogen atom, a c1 -c6 alkyl group or a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--L--R3 (wherein L is as defined above, and R3 is a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--M (wherein M is a 3- to 6-membered alicyclic group containing not more than two sulfur or oxygen atoms and formed by a linkage of from 1 to 4 carbon atoms), --O--L--M (wherein L and M are as defined above), --O--L--NR4 R5 (wherein L is as defined above and each of R4 and R5 which may be the same or different is a hydrogen atom or a c1 -c6 alkyl group, or R4 and R5 form a 6-membered ring together with the adjacent nitrogen atom), --O--L--COOR4 (wherein L and R4 are as defined above), --O--CH═CH--COOR4 (wherein R4 is as defined above), --O--L--CN (wherein L is as defined above), --O--L--c(O)--R2 (wherein L and R2 are as defined above), --O--L--S(O)n --R4 (wherein L and R4 are as defined above, and n is an integer of from 0 to 2), --O--COOR4 (wherein R4 is as defined above), --O--CONR4 R5 (wherein R4 and R5 are as defined above), --OP(O)(OR4)2 (wherein R4 is as defined above), --S(O)n R1 (wherein R1 and n are as defined above), or --S(O)n --L--O--R1 (wherein L, R1 and n are as defined above);
Z is a halogen atom, a nitro group, a c1 -c3 alkoxy group, a trifluoromethyl group, a trifluoromethoxy group, a cyano group or --S(O)n R6 (wherein n is as defined above, and R6 is a c1 -c3 alkyl group or a c1 -c3 haloalkyl group);
V is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group or a c1 -c4 alkoxy group;
W is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group, a c1 -c4 haloalkyl group, a c1 -c4 alkoxy group, a c2 -c6 alkoxyalkyl group, a c2 -c5 alkoxycarbonyl group, a c1 -c3 haloalkoxy group, a nitro group, a cyano group or --S(O)n --R6 (wherein n and R6 are as defined above); and
Q is selected from the group consisting of CH2 NHCH2 CH═CH2, CH2 NMeCH2 CH═CH2, CH2 NHAc, CH2 NHCOEt, CH2 NHCO2 Me, CH2 NHCO2 Et, CH2 NMeCO2 Me, COCH2 Cl, COCHCl2, COCCl3, COCF3, COCH2 OMe, COCH2 OPh, COCH2 CH═CHCH3, CONHMe, CONMe2, CONHEt, CONEt2, CONPr-n2, CON(CH2 CH═CH2)2, CONMePh, ##STR56## CO2 CH2 Ph, SO2 CH2 CH═CH2, SO2 CF3, P(═S)(OMe)2, P(═S)(OEt)2, P(═O)(OCH2 CH═CH2)2, P(═O)OPhOCH2 CH═CH2 ; and salts thereof.
1. A pyrazole derivative of the formula I
wherein
A is a c1 -c4 alkyl group, a c2 -c4 alkenyl group or a c2 -c4 alkynyl group;
B is a hydrogen atom, a c1 -c3 alkyl group, a halogen atom, a c1 -c3 haloalkyl group, a c1 -c3 alkoxy group, a c1 -c3 alkylthio group, a c2 -c4 alkoxyalkyl group, a c2 -c4 alkylthioalkyl group or a c2 -c4 alkoxycarbonyl group;
X is a c1 -c6 alkyl group, a c1 -c6 alkoxy group, a halogen atom, a nitro group, a cyano group, a c1 -c6 haloalkyl group, a c2 -c6 alkoxyalkyl group, a c2 -c6 alkylcarbonyl group, a c2 -c6 alkoxycarbonyl group, an aminocarbonyl group substituted independently by hydrogen or by a c1 -c6 alkyl group, a c1 -c6 haloalkoxy group, a c1 -c6 alkylthio group or a c2 -c6 alkylthioalkyl group;
Y is --OR1 (wherein R1 is a c3 -c8 cycloalkyl group, a c4 -c8 cycloalkylalkyl group, a c3 -c6 alkenyl group, a c2 -c6 alkynyl group, a c1 -c6 haloalkyl group, a c3 -c8 halocycloalkylalkyl group, a c3 -c6 haloalkenyl group, a c2 -c6 haloalkynyl group, or a c2 -c6 nitroalkyl group) a c2 -c6 nitroalkyl group or a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--L--O--R1 (wherein L is a c1 -c6 alkylene group which may be substituted by a c1 -c3 alkyl group, and R1 is as defined above), --O--L--OH (wherein L is as defined above), --O--L--O--L--O--R2 (wherein L is as defined above, and R2 is a hydrogen atom, a c1 -c6 alkyl group or a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--L--R3 (wherein L is as defined above, and R3 is a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group Or a c1 -c3 alkoxy group), --O--M (wherein M is a 3- to 6-membered alicyclic group containing not more than two sulfur or oxygen atoms and formed by a linkage of from 1 to 4 carbon atoms), --O--L--M (wherein L and M are as defined above), --O--L--NR4 R5 (wherein L is as defined above and each of R4 and R5 which may be the same or different is a hydrogen atom or a c1 -c6 alkyl group, or R4 and R5 form a 6-membered ring together with the adjacent nitrogen atom), --O--L--COOR4 (wherein L and R4 are as defined above), --O--CH═CH--COOR4 (wherein R4 is as defined above), --O--L--CN (wherein L is as defined above), --O--L--c(O)--R2 (wherein L and R2 are as defined above), --O--L--S(O)n --R4 (wherein L and R4 are as defined above, and n is an integer of from 0 to 2), --O--COOR4 (wherein R4 are as defined above), --O--CONR4 R5 (wherein R 4 and R5 are as defined above), or --OP(O)(OR4)2 (wherein R4 is as defined above), --S(O)n R1 (wherein R1 and n are as defined above), or --S(O)n --L--O--R1 (wherein L, R1 and n are as defined above);
Z is a halogen atom, a nitro group, a c1 -c3 alkoxy group, a trifluoromethyl group, a trifluoromethoxy group, a cyano group or --S(O)n R6 (wherein n is as defined above, and R6 is a c1 -c3 alkyl group or a c1 -c3 haloalkyl group);
V is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group or a c1 -c4 alkoxy group;
W is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group, a c1 -c4 haloalkyl group, a c1 -c4 alkoxy group, a c2 -c6 alkoxyalkyl group, a c2 -c5 alkoxycarbonyl group, a c1 -c3 haloalkoxy group, a nitro group, a cyano group or --S(O)n --R6 (wherein n and R6 are as defined above) and
Q is a hydrogen atom, a c1 -c6 alkyl group which may be substituted by a halogen atom, a c1 -c6 alkenyl group which may be substituted by a halogen atom, a c1 -c6 alkynyl group which may be substituted by a halogen atom, a cyanomethyl group, --c(O)--R7 (wherein R7 is a phenyl group which may be substituted by the same or different substituents selected from the group consisting of a c1 -c6 alkyl group, a c1 -c6 alkenyl group, a c1 -c6 alkynyl group, a c1 -c6 haloalkyl group, a c1 -c6 haloalkenyl group, a c1 -c6 haloalkynyl group, a halogen atom, a nitro group and a trifluoromethyl group, a c1 -c6 alkyl group, a c1 -c6 alkoxy group, or a hydroxyl group), --S(O)2 R7 (wherein R7 is as defined above), --P(O)(OR7)2 (wherein R7 is as defined above), --L--c(O)--R7 (wherein L and R7 are as defined above), --L--c(O)--N(R8)(R9) (wherein L is as defined above, and each of R8 and R9 which may be the same or different is a hydrogen atom or a c1 -c6 alkyl group), --L--R10 (wherein L is as defined above, and R10 is a phenyl group which may be substituted by the same or different substituents selected from the group consisting of a halogen atom, a nitro group and a trifluoromethyl group, a c1 -c6 alkyl group, a c1 -c6 alkoxy group, or a hydroxyl group), --L--N(R8)(R9) (wherein L, R8 and R9 are as defined above), --L--OR11 (wherein L is as defined above, and R11 is a hydrogen atom, a c1 -c6 alkyl group, or a c1 -c6 alkenyl group), --L--OC(O)R12 (wherein L is as defined above, and R12 is a c1 -c6 alkyl group or a c1 -c6 alkoxy group), --L--S(O)n R11 (wherein L, n and R11 are as defined above), --L--SC(O)R8 (wherein L and R8 are as defined above), ##STR42## (wherein each of L1 and L2 which may be the same or different is a methylene group, an oxygen atom or a sulfur atom, R12 is a hydrogen atom or a c1 -c3 alkyl group, and m is 2 or 3); and a salt thereof.
6. A pyrazole derivative of the formula I ##STR57## wherein
A is a c1 -c4 -group, a c2 -c4 -alkenyl group, or a c2 -c4 alkynyl group;
B is a hydrogen, a c1 -c3 alkyl group, a halogen atom, a c1 -c3 -haloalkyl group, a c1 -c3 -alkoxy group, a c1 -c3 -alkylthio group, a c2 -c4 -alkoxyalkyl group, a c2 -c4 -alkylthioalkyl group or c2 -c4 -alkoxycarbonyl group;
X is a c1 -c6 -alkyl group, a c1 -c6 -alkoxy group, a halogen atom, a nitro group, a cyano group, a c1 -c6 -haloalkyl group, a c2 -c6 -alkoxyalkyl group, a c2 -c6 -alkylcarbonyl group, a c2 -c6 -alkoxycarbonyl group, an aminocarbonyl group substituted independently by hydrogen or by a c1 -c6 -alkyl group, a c1 -c6 -haloalkoxy group, a c1 -c6 -alkylthio group or a c2 -c6 -alkylthioalkyl group;
Y is --OR1 (wherein R1 is a c3 -c8 -cycloalkyl group, a c4 -c8 -cycloalkylalkyl group, a c3 -c6 -alkenyl group, a c2 -c6 -alkynyl group, a c1 -c6 haloalkyl group, a c3 -c8 -halocycloalkylalkyl group, a c3 -c6 haloalkenyl group, a c2 -c6 haloalkynyl group, or a c2 -c6 nitroalkyl group), --O--L--O--R (wherein L is a c1 -c6 alkylene gorup which may be substituted by a c1 -c3 alkyl group, and R is a c1 -c4 alkyl group), --O--L--O--R1 (wherein L is a c1 -c6 alkylene group which may be substituted by a c1 -c3 -alkyl group, and R1 is as defined above), --O--L--OH (wherein L is as defined above), O--L--O--L--O--R2 (wherein L is as defined above, and R2 is a hydrogen atom, a c1 -c6 alkyl group or a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--L--R3 (wherein L is as deined above, and R3 is a phenyl group which may be substituted by a c1 -c3 alkyl group, a halogen atom, a nitro group or a c1 -c3 alkoxy group), --O--M (wherein M is a 3- to 6-membered alicyclic group containing not more than two sulfur or oxygen atoms and formed by a linkage of from 1 to 4 carbon atoms), O--L--M (wherein L and M are as defined above), --O--L--NR4 R5 (wherein L is as defined above and each of R4 and R5 which may be the same or different is a hydrogen atom or a c1 -c 6 alkyl group, or R4 and R5 form a 6-membered ring together with the adjacent nitrogen atom), --O--L--COOR4 (wherein L and R4 are as defined above), --O--CH═CH--COOR4 (wherein R4 is as defined above), --O--L--CN (wherein L is as defined above)--O--L--c(O)--R2 (wherein L and R2 are as defined above), --O--L--S(O)n --R4 (wherein L and R4 are as defined above, and n is an integer of from 0 to 2) --O--COOR4 (wherein R4 are as defined above), --O--CONR4 R5 (wherein R4 and R5 are as defined above, or --OP(O)(OR4)2 (wherein R4 is as defined above);
Z is a halogen atom, a nitro group, a c1 -c3 alkoxy group, a trifluoromethylgroup, a trifluoromethoxy group, a cyano group or --S(O)n R6 (wherein n is as defined above, and R6 is a c1 -c3 alkyl group or a c1 -c3 haloalkyl group);
V is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group or a c1 -c4 alkoxy group;
W is a hydrogen atom, a halogen atom, a c1 -c4 alkyl group, a c1 -c4 haloalkyl group, a c1 -c4 alkoxy group, a c2 -c6 alkoxyalkyl group, a c2 -c5 alkoxycarbonyl group, a c1 -c3 haloalkoxy group, a nitro group, a cyano group or --S(O)n --R6 (wherein n and R6 are as defined above) and
O is a hydrogen atom, a c1 -c6 alkyl group which may be substituted by a halogen atom, a c1 -c6 alkenyl group which may be substituted by a halogen atom, a c1 -c6 alkynyl group which may be substituted by a halogen atom, a cyanomethyl group --c(O)--R7 (wherein R7 is a phenyl group which may be substituted by the same or different substituents selected from the group consisting of a c1 -c6 alkyl group, a c1 -c6 alkenyl group, a c1 -c6 alkynyl group, a c1 -c6 haloalkyl group, a c1 -c6 haloalkenyl group, a c1 -c6 haloalkynyl group, a halogen atom, a nitro group and a trifluoromethyl group, a c1 -c6 alkyl group, a c1 -c6 alkoxy group, or a hydroxyl group), --S(O)2 R7 (wherein R7 is as defined above), --P(O)(OR7)2 (wherein R7 is as defined above, --L--c(O)--R7 (wherein L and R7 are as defined above, --L--c--(O)--N(R8)(R9)(wherein L is as defined above, and each of R8 and R9 which may be the same or different is a hydrogen atom or a c1 -c6 alkyl group), --L--R10 (wherein L is as defined above, and R10 is a phenyl group which may be substituted by the same or different substituents selected from the group consisting of a halogen atom, a nitro group and a trifluoromethyl group, a c1 -c6 alkyl group, a c1 -c6 alkoxy group, or a hydroxy group), --L--N(R8)(R9) (wherein L, R8 and R9 are as defined above), --L--OR11 (wherein L is as defined above, and R11 is a hydrogen atom, a c1 -c6 alkyl group, or a c1 -c6 alkenyl group), --L--OC(O)R12 (wherein L is as defined above, and R12 is a c1 -c6 alkyl group or a c1 -c6 alkoxy group), --L--S(O)n R11 (wherein L, n and R11 are as defined above, --L--SC(O)R8 (wherein L and R8 are as defined above), ##STR58## (wherein each of L1 and L2 which may be the same or different is a methylene group, an oxygen atom or a sulfur atom, R12 is a hydrogen atom or a c1 -c3 alkyl gropu, and m is 2 or 3); and a salt thereof.
2. The A pyrazole derivative of the formula I according to claim 1, ##STR43## wherein A, B, X, Y, Z and Q are as follows:
A: Me, Et, n-Pr, i-Pr, CH2 CH═CH2, CH2 c.tbd.CH, t-Bu
B: H, Me, Et, n-Pr, i-Pr, Cl, Br, CH2 Cl, CF3, OMe, OEt, OPr-i, SMe, CH2 OMe, CH2 SMe, CO2 Me, CO2 Et
X: Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, S-Bu, t-Bu, OMe, OEt, OPr-n, OPr-i, OBu-n, OBu-i, OBu-s, OBu-t, F, Cl, Br, I, NO2, CN, CH2 F, CHF2, CF3, CH2 CF3, CHCl, CCl3, CHClMe, CH2 CH2 Cl, CHClCH2 Cl, CH2 Br, CHBrMe, CH2 CH2 Br, CH2 CH2 Br, CH2 OMe, CH2 OEt, CH2 OPr-n, CH2 OPr-i, CH2 OBu-n, CH2 OBu-i, CH2 OBu-s, CH2 OBu-t, CHMeOMe, CHMeOEt, CHMeOPr-n, CHMeOPr-i, CHMeOBu-n, CHMeOBu-i, CHMeOBu-s, CHMeOBu-t, CH2 CH2 OMe, CH2 CH2 OEt, CH2 CH2 OPr-i, Ac, COEt, COPr-n, COPr-i, COOMe, COOEt, COOPr-i, CONHMe, CONHEt, CONMe2, CONEt2, CONEtMe, OCHF2, OCF3, OCH2 CF3, SMe, SEt, CH2 SMe, CH2 SEt, CHMeSMe, CHMeSEt
Y: ##STR44## OCHMeCH═CH2, OCMe2 CH═CH2, OCH2 CMe═CH2, OCH2 CH═CHMe, OCH2 CH═CMe2, OCH2 c.tbd.CH, OCHMeC.tbd.CH, OCMe2 c.tbd.CH, OCH2 c.tbd.CMe, OCH2 CH2 F, OCH2 CHF2, OCH2 CF3, OCH2 CH2 Cl, OCHMeCH2 Cl, OCH2 CCl3, OCH2 CH2 CH2 Cl, OCH2 CH2 Br, ##STR45## OCH2 CCl═CH2, OCH2 CH2 CH═CH2, OCH2 CCl═CHCl, OCH2 CH2 NO2, OPh, OPh-Me-2 OPh-Cl-4, OPh-NO2 -4, OCH2 CH2 OMe, OCH2 CH2 OEt, OCH2 CH2 OPr-n, OCH2 CH2 OPr-i, OCH2 CH2 OBu-N, OCH2 CH2 OBu-i, OCH2 CH2 Bu-s, OCH2 CH2 OBu-t, OCHMeCH2 OMe, OCH2 CH2 OPh, OCH2 CH2 OCH2 CH2 OMe, OCH2 CH2 OH, OCH2 CH2 OCHMeCH2 OMe, OCH2 Ph, OCHMePh, OCH2 Ph-4-Me, OCH2 Ph-4-Cl, OCH2 CH2 Ph, ##STR46## OCH2 CH2 NH2, OCH2 CH2 NHMe, OCH2 CH2 NMe2, OCH2 CH2 NEt2, ##STR47## OCH2 COOMe, OCH2 COOEt, OCH2 COOPr-n, OCH2 COOPr-i, OCH2 COOBu-t, OCHMeCOOMe, OCHMeCOOEt OCHMeCOOPr-n, OCHMeCOOPr-i, OCHMeCOOBu-t, OCH2 CH2 CN, OCH2 CN, OCHMeCN, OCH2 SMe, OCH2 c(O)Ph, OCH2 c(O)Me, OCH2 CH2 SMe, OCH2 CH2 SOMe, OCH2 CH2 SO2 Me, OCH2 CH2 SEt, OCH2 CH2 SO2 Et, OCOOMe, OCOOEt, OCOOPr-i, OCONH2, OCONHMe, OCONMe2, OP(O)(OMe)2, OP(O)(OEt)2, ##STR48## SCH2 CH═CH2, SCH2 c.tbd.CH, SCH2 CF3, SCH2 CH2 Cl, SCH2 CCl3, ##STR49## SPh,SCH2 CH2 OMe, SCH2 CH2 OEt, SCH2 CH2 OPr-i, SCH2 CH2 OPh, ##STR50## S(O)CH2 CH═CH2, 2CH.tbd.CH, S(O)CH2 CF3, S(O)CH2 CH2 Cl, S(O)CH2 ##STR51## S(O)Ph, S(O)CH2 CH2 OMe, S(O)CH2 CH2 OEt, S(O)CH2 CH2 OPr-i, S(O)CH2 CH2 OPh, ##STR52## SO2 CH2 CH═CH2, SO2 CH2 c.tbd.CH, SO2 CH2 CF3, SO2 CH2 CH2 Cl, SO2 CH2 ##STR53## SO2 Ph, SO2 CH2 CH2 OMe, SO2 CH2 CH2 OEt, SO2 CH2 CH2 OPr-i,
Z: F, Cl, Br, I, NO2, OMe, OEt, OPr-n, OPr-I, CF3, CN, SMe, SOMe, SO2 Me, SCF3, SOCF3, SO2 CF3
Q H, Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, s-Bu, t-Bu, CH2 CH2 Cl, CH2 CF3, CHClMe, CH2 CH2 Br, CHClCH2 Cl, CH2 CH═CH2, CH2 CMe═CH2, CH2 CH=CHMe, CH2 c.tbd.CH, CH2 CCl═CH2, CH2 CN, CH2 Ph, CH2 Ph-Cl-2, CH2 Ph-Cl-3, CH2 Ph-Me-2, ##STR54## CH2 Ph-Me2 -2,4, CH2 Ph-Me-4, CHMePh, CHEtPh, CH2 Ph-NO2 -2, CH2 Ph-CF3 -3, CH2 OMe, CH2 OEt, CH2 OH, CHMeOH, CH2 NHMe, CH2 NMe2, CHMeNMe2, CH2 COPh, CH2 COPh-NO2 -4, CH2 COPh-Me-4, CH2 COPh-Cl-4, CH2 COPh-Me-2,4, CH2 COPh-CF3 -4, CH2 Ac, CH2 COEt, CHMeAc, CH2 CO2 Me, CH2 CO2 Et, CH2 CO2 Pr-n, CH2 COPr-i, CH2 CO2 Bu-t, CH2 CO2 H, CHMeCO2 H, CH2 CONHMe, CH2 CONMe2, CH2 CONHEt, CH2 CONEt2, CH2 CONPr-n2, CH2 OCH2 CH═CH2, CH2 OAc, CH2 COEt, CH2 COPr-i, CH2 COBu-t, CH2 OCO2 Me, CH2 OCO2 Et, CH2 OCO2 Pr-i, CH2 OCO2 Bu-t, CH2 SMe, CH2 SEt, CH2 SCH2 CH═CH2, CH2 SAc, CH2 SCOBu-t, CH2 SO2 Me, CH2 SO2 Et, CH2 SO2 CH2 CH═CH2, COPh, COPh-Me-4, COPh-NO2 -2, COPh-Cl2 -2,4, Ac, COEt, COPr-n, COPr-i, COBu-n, COBu-t, CO2 Me, CO2 Et, CO2 Bu-t, CO2 Pr-i, CO2 Ph, SO2 Me, SO2 Et, SO2 Ph, SO2 Ph-Me-4, SO2 Ph-Cl-4, SO2 Ph-(NO2)2 -2,4, P(═O)(OMe)2, P(═O)(OEt)2, P(═O)(OPr-n)2, P(═O)(OPr-i)2, P(═O)OMeOPh;
and a salt thereof.
3. A selective herbicidal composition comprising a herbicidally effective amount of a pyrazole derivative of the formula I as defined in claim 1 or its salt and an agricultural carrier or diluent.
4. A method for controlling weeds, which comprise applying a herbicidally effective amount of a pyrazole derivative of the formula I as defined in claim 1 or its salt to a locus to be protected.
8. The pyrazole derivative of the formula I according to claim 6, wherein A is ethyl, B is hydrogen, Q is hydrogen, X is Cl, Z is SO2 Me, and Y is --O--L--O--R wherein L is a c2 alkylene group which may be substituted by a methyl group and R is a c1-4 alkyl group. 9. The pyrazole derivative of the formula I according to claim 8, wherein Y is --OCH2 CH2 OMe, --OCH2 CH2 OEt, --OCH2 CH2 OPr-n, --CH2 CH2 OPr-i, --OCH2 CH2 OBu-n, --OCH2 CH2 OBu-i, --OCH2 CH2 OBu-s, --OCH2 CH2 OBu-t, --OCMeCH2 OMe or --OCH2 CHMeOMe.
10. The pyrazole derivative of the formula I according to claim 9, wherein Y is --OCH2 CH2 OMe.

The present invention relates to novel 4-benzoylpyrazole derivatives and selective herbicides containing such derivatives as active ingredients, which are useful particularly as upland field herbicides.

Various herbicides have been developed for practical use from extensive research and development of herbicides for many years, and such herbicides have contributed to a reduction of the labor force required for controlling weeds or to improvement of the productivity of agricultural or horticultural plants.

Even now, it is still desired to develop a new herbicide having superior herbicidal properties. In particular, it is desired to develp an agricultural or horticultural herbicide which is capable of selectively controlling weeds without adversely affecting the crop plant and at a low dose. However, conventional herbicides do not necessarily provide such desired herbicidal properties.

On the other hand, certain compounds of 4-benzoylpyrazole derivatives are known to have herbicidal activities. For example, pyrazolate (common name) and pyrazoxyfen (common name) are practically used as herbicides for paddy fields. While exhibiting excellent herbicidal activities as paddy field herbicides, these compounds are not suitable as upland herbicides since their herbicidal activities are weak against weeds of upland fields. Among 4-benzoylpyrazole derivatives, it is desired to develop a superior compound useful as an upland field herbicide.

The present invention provides a pyrazole derivative having the formula: ##STR3## wherein

A is a C1 -C4 alkyl group, a C2 -C4 alkenyl group or a C2 -C4 alkynyl group;

B is a hydrogen atom, a C1 -C3 alkyl group, a halogen atom, a C1 -C3 haloalkyl group, a C1 -C3 alkoxy group, a C1 -C3 alkylthio group, a C2 -C4 alkoxyalkyl group, a C2 -C4 alkylthioaalkyl group or a C2 -C4 alkoxycarbonyl group;

X is a C1 -C6 alkyl group, a C1 -C6 alkoxy group, a halogen atom, a nitro group, a cyano group, a C1 -C6 haloalkyl group, a C2 -C6 alkoxyalkyl group, a C2 -C6 alkylcarbonyl group, a C2 -C6 alkoxycarbonyl group, an aminocarbonyl group substituted independently by hydrogen or by a C1 -C6 alkyl group, a C1 -C6 haloalkoxy group, a C1 -C6 alkylthio group or a C2 -C6 alkylthioalkyl group;

Y is --OR1 (Wherein R1 is a C3 -C8 cycloalkyl group, a C4 -C8 cycloalkylalkyl group, a C3 -C6 alkenyl group, a C2 -C6 alkynyl group, a C1 -C6 haloalkyl group, a C3 C8 halocycloalkylalkyl group, a C3 -C6 haloalkenyl group, a C2 -C6 haloalkynyl group, a C2 -C6 nitroalkyl group or a phenyl group which may be substituted by a C1-C3 alkyl group, a halogen atom, a nitro group or a C1 -C3 alkoxy group), --O--L--O--R1 (Wherein L is a C1 -C6 alkylene group which may be substituted by a C1 -C3 alkyl group, and R1 is as defined above), --O--L--OH (wherein L is as defined above), --O--L--O--L--O--R2 (wherein L is as defined above, and R2 is a hydrogen atom, a C1 -C6 alkyl group or a phenyl group which may be substituted by a C1 -C3 alkyl group, a halogen atom, a nitro group or a C1 -C3 alkoxy group), --O--L--R3 (wherein L is as defined above, and R3 is a phenyl group which may be substituted by a C1 -C3 alkyl group, a halogen atom, a nitro group or a C1 -C3 alkoxy group), --O--M (wherein M is a 3- to 6-membered alicyclic group containing not more than two sulfur or oxygen atoms and formed by a linkage of from 1 to 4 carbon atoms), --O--L--M (wherein L and M are as defined above), --O--L--NR4 R5 (wherein L is as defined above and each of R4 and R5 which may be the same or different is a hydrogen atom or a C1 -C6 alkyl group, or R4 and R5 form a ring together with the adjacent nitrogen atom), --O--L-COOR4 (wherein L and R4 are as defined above), --O--CH═CH--COOR4 (wherein R4 is as defined above), --O--L--CN (wherein L is as defined above), --O--L--C(O)--R2 (wherein L and R2 are as defined above), --O--L--S(O)n --R4 (wherein L and R4 are as defined above, and n is an integer of from 0 to 2), --O--COOR4 (wherein R4 are as defined above), --O--CONR4 R5 (wherein R4 and R5 are as defined above), --OP(O)(OR4)2 (wherein R4 is as defined above), --S(O)n R1 (wherein R1 and n are as defined above), or --S(O)n --L--O--R1 (wherein L, R1 and n are as defined above);

Z is a halogen atom, a nitro group, a C1 -C3 alkoxy group, a trifluoromethyl group, a trifluoromethoxy group, a cyano group or --S(O)n R6 (wherein n is as defined above, and R6 is a C1 -C3 alkyl group or a C1 -C3 haloalkyl group);

V is a hydrogen atom, a halogen atom, a C1 -C4 alkyl group or a C1 -C4 alkoxy group;

W is a hydrogen atom, a halogen atom, a C1 -C4 alkyl group, a C1 -C4 haloalkyl group, a C1 -C4 alkoxy group, a C2 -C6 alkoxyalkyl group, a C2 -C5 alkoxycarbonyl group, a C1 -C3 haloalkoxy group, a nitro group, a cyano group or --S(O)n --R6 (wherein n and R6 are as defined above); and

Q is a hydrogen atom, a C1 --C6 alkyl group which may be substituted by a halogen atom, a C1 -C6 alkenyl group which may be substituted by a halogen atom, a C1 -C6 alkynyl group which may be substituted by a halogen atom, a cyanomethyl group, --C(O)--R7 (wherein R7 is a phenyl group which may be substituted by the same or different substituents selected from the group consisting of a C1 -C6 alkyl group, a C1 -C6 alkenyl group, a C1 -C6 alkynyl group, a C1 -C6 haloalkyl group, a C1 -C6 haloalkenyl group, a C1 -C6 haloalkynyl group, a halogen atom, a nitro group and a trifluoromethyl group, a C1 -C6 alkyl group, a C1 -C6 alkoxy group, or a hydroxyl group), --S(O)2 R7 (wherein R7 is as defined above), --P(O)(OR7)2 (wherein R7 is as defined above), --L--C(O)--R7 (wherein L and R7 are as defined above), --L--C(O)--N(R8)(R9) (wherein L is as defined above, and each of R8 and R9 which may be the same or different is a hydrogen atom or a C1 -C6 alkyl group), --L--R10 (wherein L is as defined above, and R10 is a phenyl group which may be substituted by the sam or different substituents selected from the group consisting of a halogen atom, a nitro group and a trifluoromethyl group, a C1 -C6 alkyl group, a C1 -C6 alkoxy group, or a hydroxyl group), --L--N(R8)(R9) (wherein L, R8 and R9 are as defined above), --L--OR11 (wherein L is as defined above, and R11 is a hydrogen atom, a C1 -C6 alkyl group, or a C1 -C6 alkenyl group), --L--OC(O)R12 (wherein L is as defined above, and R12 is a C1 -C6 alkyl group or a C1 C6 alkoxy group), --L--S(O)n R11 (wherein L, n and R11 are as defined above), --L--SC(O)R8 (wherein L and R8 are as defined above), ##STR4## (wherein each of L1 and L2 which may be the same or different is a methylene group, an oxygen atom or a sulfur atom, R12 is a hydrogen atom or a C1 -C3 alkyl group, and m is 2 or 3); and a salt thereof.

The present invention also provides a selective herbicidal composition comprising a herbicidally effective amount of at least one pyrazole derivative of the formula I as defined above or its salt and an agricultural carrier or diluent.

Further, the present invention provides a method for selectively controlling weeds, which comprises applying the pyrazole derivative of the formula I as defined above or its salt to the locus to be protected.

Furthermore, the present invention provides a substituted benzene derivative of the formula: ##STR5## wherein G is a carboxyl group, a halocarbonyl group or a cyanocarbonyl group, and X, Y, Z, V and W are as defined above.

Now, the present invention will be described in detail with reference to the preferred embodiments.

In the compound of the formula I of the present inveniton, A, B, X, Y, Z and Q are preferably selected from the following substituents, respectively:

A:Me, Et, n-Pr, i-Pr, CH2 CH═CH2, CH2 C.tbd.CH, t-Bu

B:H, Me, Et, n-Pr, i-Pr, Cl, Br, CH2 Cl, CF3, OMe, OEt, OPr-i, SMe, CH2 OMe, CH2 SMe, CO2 Me, CO2 Et

X:Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, s-Bu, t-Bu, OMe, OEt, OPr-n, OPr-n, OPr-i, OBu-n, OBu-i, OBU-s, OBu-t, F, Cl, Br, I, NO2 CN, CH2 F, CHF2, CF3, CH2 CF3, CH2 Cl, CCl3, CHClMe, CH2 CH2 Cl, CHClCH2 Cl, CH2 Br, CHBrMe, CH2 CH2 Br, CH2 OMe, CH2 OEt, CH2 OPr-n, CH2 OPr-i, CH2 OBu-n, CH2 OBu-i, CH2 OBu-s, CH2 OBu-t, CHMeOMe, CHMiOEt, CHMeOPr-n, CHMeOPr-i, CHMeOBu-n, CHMeOBu-i, CHMeObu-s, CHMeOBu-t, CH2 CH2 OMe, CH2 CH2 OEt, CH2 CH2 OPr-i, Ac, COEt, COPr-n, COPr-i, COOMe, COOEt, COOPr-i, CONHMe, CONHEt, CONMe2, CONEt2, CONEtMe, OCHF2, OCF3, OCH2 CF3, SMe, SEt, CH2 SMe, CH2 SEt, CHMeSMe, CHMeSEt

Y: ##STR6## OCHMeCH═CH2, OCMe2 CH═CH2, OCH2 CMe═CH2, OCH2 CH═CHMe, OCH2 CH═CMe2, OCH2 C.tbd.CH, OCHMeC.tbd.CH, OCHMe2 C.tbd.CH, OCH2 .tbd.CMe, OCH2 CH2 F, OCH2 CHF2, OCH2 CF3, OCH2 CH2 Cl, OCHMeCH2 Cl, OCH2 CCl3, OCH2 CH2 CH2 Cl, OCH2 CH2 Br, ##STR7## OCH2 CCl═CH2, OCH2 CH2 CH═CH2, OCH2 CCl═CHCl, OCH2 CH2 NO2, OPh,OPh-Me-2 OPh-Cl-4, OPh-NO2 -4, OPH2 CH2 OMe, OCH2 CH2 OEt, OCH2 CH2 OPr-n, OCH2 CH2 OPr-i, OCH2 CH2 OBu-n, OCH2 CH2 OBu-i, OCH2 CH2 Bu-s, OCH2 CH2 OBu-t, OCHMeCH2 OMe, OCH2 CH2 OPh, OCH2 CH2 OCH2 CH2 OMe, OCH2 CH2 OH, OCH2 CH2 OCHMeCH2 OMe, OCH2 Ph, OCHMePh, OCH2 Ph-4-Me, OCH2 Ph-4-Cl, OCH2 CH2 Ph, ##STR8## OCH2 CH2 NH2, OCH2 CH2 NHMe, OCH2 CH2 NMe2, OCH2 CH2 NEt2, OCH2 COOMe, OCH2 COOEt, OCH2 COOPr-n, OCH2 COOPr-i, OCH2 COOBu-t, OCHMeCOOMe, OCHMeCOOEt OCHMeCOOPr-n, OCHMeCOOPr-i, OCHMeCOOBu-t OCH2 CH2 CN, OCH2 CN, OCHMeCN, OCH2 SMe, OCH2 C(O)Ph, OCH2 C(O)Me, OCH2 CH2 SMe, OCH2 CH2 SOMe, OCH2 CH2 SO2 Me, OCH2 CH2 SEt, OCH2 CH2 SO2 Et, OCOOMe, OCOOEt, OCOOPr-i, OCONH2, OCONHMe, OCONMe2, OP(O)(OMe)2, OP(O)(OEt)2, ##STR9## SCH2 CH═CH2, SCH2 C.tbd.CH, SCH2 CF3, SCH2 CH2 Cl, SCH2 CCl3, ##STR10## SPh, SCH2 CH2 OMe, SCH2 CH2 OEt, SCH2 CH2 OPr-i, SCH2 CH2 OPh, ##STR11## S(O)CH2 ═CH2, S(O)CH2 CH.tbd.CH,S(O)CH2 CF3, S(O)CH2 CH2 Cl, ##STR12## S(O)Ph, S(O)CH2 CH2 OMe, S(O)CH2 CH2 OEt, S(O)CH2 CH2 OPr-i, S(O)CH2 CH2 OPh, ##STR13## SO2 CH2 CH═CH2, SO2 CH2 C.tbd.CH, SO2 CH2 CF3, SO2 CH2 CH2 Cl, SO2 CH2 ##STR14## SO2 Ph, SO2 CH2 CH2 OMe, SO2 CH2 CH2 OEt, SO2 CH2 CH2 OPr-i, Z : F, Cl, Br, I, NO2, OMe, OEt, OPr-n, OPr-i, CF3, CN, SMe, SOMe, SO2 Me, SCF3, SOCF3, SO2 CF3 .

Q : H, Me, Et, n-Pr, i-Pr, n-Bu, i-Bu, s-Bu, t-Bu, CH2 CH2 Cl, CH2 CF3, CHClMe, CH2 CH2 Br, CHClCH2 Cl, CH2 CH═CH2, CH2 CME═CH2, CH2 CH═CHMe, CH2 C.tbd.CH, CH2 CCl═CH2, CH2 CN, CH2 Ph, CH2 Ph-Cl-2, CH2 Ph-Cl-3, CH2 Ph-Me-2, ##STR15## CH2 Ph-Me2 -2,4, CH2 Ph-Me-4, CHMePh, CHEtPh, CH2 Ph-NO2 -2, CH2 Ph-CF3 -3, CH2 OMe, CH2 OEt, CH2 OH, CHMeOH, CH2 NHMe, CH2 NMe2, CHMeNM2, CH2 COPh, CH2 COPh-NO2 -4, CH2 COPh-Me-4, CH2 COPh-Cl-4, CH2 COPh-Me2 -2,4, CH2 COPh-CF3 -4, CH2 Ac, CH2 COEt, CHMeAc, CH2 CO2 Me, CH2 CO2 Et, CH2 CO2 Pr-n, CH2 CO2 Pr-i, CH2 CO2 Bu-t, CH2 CO2 H, CHMeCO2 H, CH2 CONHMe, CH2 CONMe2, CH2 CONHEt, CH2 CONEt2, CH2 CONPr-n2, CH2 OCH2 CH═CH2, CH2 OAc, CH2 COEt, CH2 COPr-i, CH2 COBu-t, CH2 OCO2 Me, CH2 OCO2 Et, CH2 OCO2 Pr-i, CH2 OCO2 Bu-t, CH2 SMe, CH2 SEt, CH2 SCH2 CH═CH2, CH2 SAc, CH2 SCOBu-t, CH2 SO2 Me, CH2 SO2 Et, CH2 SO2 CH2 CH═CH2, CH2 NHCH2 CH═CH2, CH2 NMeCH2 CH═CH2, CH2 NHAc, CH2 NHCOEt, CH2 NHCO2 Me, CH2 NHCO2 Et, CH2 NMeCO2 Me, COPh, COPh-Me- 4, COPh-NO2 -2, COPh-Cl2 -2,4, Ac, COEt, COPr-n, COPr-i, COBu-n, COBu-t, COCH2 Cl, COCHCl2, COCCl3, COCF3, COCH2 OMe, COCH2 OPh, COCH2 CH═CHCH3, CO2 Me, CO2 Et, CO2 Bu-t, CO2 Pr-i, CONHMe, CONMe2, CONHEt, CONEt2, CONPr-n2, CON(CH2 CH═CH2)2, CONMePh, ##STR16## CO2 CH2 Ph, CO2 Ph, SO2 Me, SO2 Et, SO2 CH2 CH═CH2, SO2 Ph, SO2 Ph-Me-4, SO2 Ph-Cl-4, SO2 Ph-(NO2)2 -2,4 SO2 CF3, P(═O)(OMe)2, P(═O)(OEt)2, P(═O)(OPr-n)2, P(═O)(OPr-i)2, P(═S)(OMe)2, P(═S)(OEt)2, P(═O)OMeOPh, P(═O)(OCH2 CH═CH2)2, P(═O)OPhOCH2 CH═CH2

When Q is a hydrogen atom, the compound may readily from a salt with a metal or with an organic base.

As such a metal, sodium, potassium, calcium, lithium, barium, magnesium, iron, copper, nickel or manganese may be mentioned.

As such an organic base, methylamine, dimethylamine, trimethylamine, ethylamine, diethylamine, triethylamine, n-propylamine, di-n-propylamine, i-propylamine, di-i-propylamine, n-butylamine, i-butylamine, sec-butylamine, tert-butylamine, piperidine, pyrrolidine, morpholine, pyridine, N,N-dimethylaniline or choline may be mentioned.

In the course of researches on the herbicidal properties of various organic compounds with an aim to develop useful herbicides, the present inventors have found that the above-mentioned compound of the present invention exhibits excellent herbicidal activities against narrow leaf weeds (gramineous and cyperaceous weeds) and against broad leaf weeds and no substantial phytotoxicity against useful plants e.g. crop plants such as Zea mays (corn), Sorghum bicolor (sorgo), Triticum spp (wheat) and Hordeum vulgare (barley). The present invention has been accomplished on the basis of this discovery.

The compound of the present invention exhibits strong herbicidal activities in each of soil treatment, soil incorporation treatment and foliage treatment. On the other hand, it exhibits no phytotoxicity against crop plants such as Zea mays, Sorghum bicolor, Triticum spp and Hordeum vulgare in a practical application in any of soil treatment, soil incorporation treatment and foliage treatment. Thus, the compound of the present invention has high selectivity and it is extremely effective for controlling weeds during the cultivation of these crop plants. Namely, the compound of the present invention exhibits strong herbicidal activities against noxious weeds such as Setaria viridis (green foxtail), Echinochloa crus-galli (barnyardgrass), Amarathus lividus (livid amaranth), Polvgonum longisetum (persicaria blumei gross), Xanthium strumarium (cocklebur), Abutilon theophrasti (velvet leaf) and Cyperus esculentus (yellow nutsedge), which develop during the cultivation of Zea mays or Sorphum bicolor. The herbicidal activities against gramineous weeds and Cyperus esculentus are remarkablly high and extremely unique. Heretofore, during the cultivation of Zea mays or Sorghum bicolor, it has been common to employ atranzine or cyanazine as a triazine-type herbicide, or alachlor or metolachlor as an acid anilide type herbicide. However, atranzine and cyanazine have poor herbicidal activities against gramineous weeds although they show high activities against broad leaf weeds, and their activities against Cyperus esculentus are very low. On the other hand, alachlor and metolachlor have poor activities against broad leaf weeds although their activities against gramineous weeds are high, and their activities against Cyperus esculentus are very poor. Thus, it has been difficult to eradicate all the weed species by a single application of such herbicides.

As a result of various studies, the present inventors have found the compound of the present invention which exhibits excellent herbicidal effects against a wide range of weeds, and the present invention has been accomplished on the basis of this discovery. The compound of the present invention also has a feature that it exhibits no phytotoxicity against crop plants such as Zea mays, Sorqhum bicolor, Triticum spp and Hordeum vulgare and thus can safely be applied to the fields for such crop plants.

Further, the compound of the present invention includes a compound which shows selectivity between Oryza sativa (rice) and Echinochloa crus-qalli (barnyardgrass), and it also includes a compound having selectivity for a useful plant such as Goxxypium spp (cotton), Beta vulgaris (sugar beat) or Clycine max (soybean).

Heretofore, it has been known that 4-benzoylpyrazole derivatives have excellent herbicidal activities. For example, pyrazolate (common name) is commercially available and widely used for practical application. However, such conventional herbicides are restricted in their application to paddy fields, and their activities are very poor in their application to upland fields. Whereas, as a result of extensive research for many years on 4-benzoylpyrazole derivatives, the present inventors have finally found that the compound of the present invention which simultaneously satisfies the various conditions for substituents in the structure as specified above, exhibits strong herbicidal activities in the application to upland fields in each of soil treatment, soil incorporation treatment and foliage treatment. It has been found that the compound of the present invention exhibits particularly high activities against gramineous weeds and Cyperus esculentus.

The compound of the present invention can readily be prepared by any one of the following reactions. ##STR17##

In the above formulas, A, B, V, W, X, Y, Z and Q are as defined above, E is a halogen atom, a methanesulfonyloxy group or a p-toluenesulfonyloxy group. Further, ##STR18## and may be represented by either formula.

Reaction scheme (1) represents a reaction wherein benzoic acid having suitable substituents and 5-hydroxypyrazole are reacted in an inert solvent in the presence of a condensation agent and a base to obtain 4-benzoyl-5-hydroxypyrazole. The condensation agent is used in an amount of from 1.0 to 1.5 mols per mol of the benzoic acid and pyrazole. As the condensation agent, N,N'-dicyclohexylcarbodiimide may be mentioned. The solvent may be any aolvent so long as it is inert to the reaction. Particularly preferred is tert-butyl alcohol, tert-amyl alcohol or isopropyl alcohol. The base may not necessarily be required. However, in general, the yield can be improved by using a base. There is no particular restriction as to the base, but potassium carbonate or sodium carbonate may preferably be employed. The reaction temperature may range from room temperature to boiling point of the solvent, but is peferably from 50° to 100°C

The reaction time is usually from 0.5 to 20 hours.

Reaction scheme (2) shows a reaction wherein benzoyl chloride having suitable substituents and 5-hydroxypyrazole are reacted to form a benzoyl ester, which is then rearranged to a 4-benzoyl compound.

The benzoyl esterification can be accomplished in an inert solvent (such as an aromatic hydrocarbon, a fatty acid ester, a halogenated hydrocarbon, an ether, acetonitrile, dimethylsulfoxide or N,N'-dimethylformamide) or in a two phase system with such a solvent and water or in a mixture of such solvents in the presence of a suitable dehydrochlorinating agent (e.g. an inorganic base such as sodium hydroxide, potassium hydroxide or sodium hydrogencarbonate, or an organic base such as pyridine or triethylamine) at a temperature of from room temperature to 100°C for from 10 minutes to 5 hours.

The rearrangement reaction can be accomplished by means of a Lewis acid such as anhydrous aluminum chloride or a base. As the base, potassium carbonate, calcium hydroxide or sodium carbonate may be used. The Lewis acid or base is used usually in an amount of from 1 to 10 mol times.

No solvent is required. However, in some cases, it is advantageous to use a solvent having a suitable boiling point to improve the operation efficiency or the yield. As such an advantageous example, use of dioxane, toluene or xylene diglyme, may be mentioned.

The reaction temperature is usually from 50° to 150°C, and the reaction time is usually from 15 minutes to 30 hours.

Reaction scheme (3) shows a reaction wherein a benzene derivative, a 5-hydroxypyrazole derivative and carbon tetrachloride are condensed in the presence of a Lewis acid in an inert solvent or in the absence of a solvent, followed by hydrolysis to obtain a 4-benzoyl-5-hydroxypyrazole derivative. As the Lewis acid, anhydrous aluminum chloride or anhydrous aluminum bromide in an amount of at least the theoretical amount for the reaction is preferred. The solvent may be of any type so long as it is inert to the reaction. However, a chlorine-type solvent such as methylene chloride, dichloroethane or tetrachloroethane is preferred. The temperature for condensation may range from 0°C to the boiling point of the solvent, but it is preferably from 10° to 80° C. The hydrolysis is conducted in the presence of hydrochloric acid or sulfuric acid. The temperature for the hydrolysis is preferably from room temperature to 100°C The time for the hydrolysis is usually from 0.1 to 10 hours.

Reaction scheme (4) shows a reaction wherein a benzoyl cyanide derivative and a 5-hydroxypyrazole derivative are reacted in the presence of a Lewis acid and a base in an inert solvent or in the absence of a solvent to obtain a 4-benzoyl-5-hydroxypyrazole. As the Lewis acid, zinc chloride, aluminum chloride or aluminum bromide may be used. As the base, pyridine or triethylamine may be mentioned. The Lewis acid and the base are used usually in an amount of from 1 to 10 mol times. As the solvent, methylene chloride, dichloroethane or tetrachloroethane may be mentioned. The reaction temperature is usually from 0° to 80°C, preferably from 10° to 50°C The reaction time is from 0.5 to 20 hours.

Reaction scheme (5) shows a reaction wherein 4-benzoyl-5-hydroxyyrazole is condensed with a halide, a methanesulfonic acid ester or a p-toluenesulfonic acid ester.

For this reaction, it is preferred to employ from 1 to 3 mol times of a dehydrohalogenating agent. As such a dehydrohalogenating agent, an inorganic base such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium hydrogencarbonate or potassium carbonate, or an organic base such as pyridine or triethylaine, may be mentioned.

There is no particular restriction as to the solvent so long as it is inert to the reaction. A wide range of solvents including an aromatic hydrocarbon, a fatty acid ester, a halogenated hydrocarbon, an ether, a ketone, an aliphatic hydrocarbon, acetonitrile, dimethylsulfoxide and dimethylformamide may be used.

The reaction temperature may be optionally selected within a range of from room temperature to the boiling point of the solvent. The reaction time is usually from 30 minutes to 30 hours.

Reaction scheme (6) shows a reaction wherein 4-benzoyl-5-hydroxypyrazole is converted to a 5 halogeno compound by a halogenating agent, or to a methanesulfonate compound or a p-toluenesulfonate compound by methane sulfonyl chloride or p-toluenesulfonyl chloride, followed by condensation with a suitable alcohol or acid.

As the halogenating agent, phosphorus oxychloride, phosphorus pentachloride or thionyl chloride may be mentioned.

As the solvent, a wide range of solvents inert to the reaction, such as dimethylformamide, may be employed. However, the reaction can be conducted without any solvent.

The reaction temperature is preferably from 30° to 150° C, and the reaction time is usually from 30 minutes to 10 hours. In some cases, the reaction time may be shortened or the yield may be improved by an addition of a dehydrohalogenating agent.

The condensation reaction with an alcohol or acid is conducted by an addition of a dehydrohalogenating agent.

As such a dehydrohalogenating agent, a base such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium alkoxide or sodium hydride may be employed.

The solvent may be any solvent which is inert to the reaction (such as an aromatic hydrocarbon, an ether, a ketone or N,N'-dimethylformamide). The reaction temperature may be selected within a range of from room temperature to the boiling point of the solvent.

The substituted benzene derivatives used as the starting materials for the compounds of the present invention have novel structures, and they may readily be prepared by a proper combination of various known syntheses. For instance, compounds wherein the substituent Z in the benzene ring is --S(O)n CH3 can be prepared in accordance with the following reaction schemes. ##STR19##

In the above formulas, X and Y are as defined above, and Hal is a halogen atom.

Now, the preparation of the substituted benzene derivatives and pyrazole derivatives will be described in detail with reference to Examples. However, it should be understood that the present invention is by no means restricted by such specific Examples.

EXAMPLE 1
PAC Preparation of 4-(2-chloro-4-methanesulfonyl-3-(2-methoxy)ethoxybenzoyl)-1-ethyl-5-hydrox ypyrazole
(1) (2-methoxy)ethyl 2-chloro-4-methanesulfonyl-3-(2-methoxy)ethoxybenzoate

1.2 g of 2-chloro-3-hydroxy-4-methanesulfonylbenzoic acid, 1.4 g of potassium carbonate and 2.1 g of 2bromoethyl methyl ether were put into 20 ml of N,N-dimethylformamide and reacted under heating at a temperture of from 60° to 70°C for from 6 to 7 hours. Then, the solvent was distilled off, and after an addition of water, the reaction mixture was extracted with chloroform. The extract was dried over anhydrous sodium sulfate, and the solvent was distilled off to obtain 1.9 g of a crude product of the above identified compound.

(2) 2 -chloro-4-methanesulfonyl-3-(2-methoxy)ethoxybenzoic acid

1.9 g of the crude product of (2-methoxy)ethyl 2-chloro-4-methanesulfonyl-3-(2-methoxy)ethoxybenzoate was dissolved in 50 ml of ethanol, and 20 ml of an aqueous solution containing 1 g of sodium hydroxide was added thereto. The mixture was stirred at room temperature for 30 minutes. Then, ethanol was distilled off, and water was added to the residue. The mixture was washed with chloroform, then acidified with concentrated hydrochloric acid and extracted with chloroform. The extract was dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain 1.4 g of a crude product of the above identified compound. To the crude product, n-hexane was added, and the mixture was left to stand, whereby the desired product was gradually crystallized. Melting point: 89°-92°C

(3) 4-(2-chloro-4-methanesulfonyl-3-(2-methoxy)ethoxybenzoyl)-1-ethyl-5-hydrox ypyrazole

1.2 g of the crude product of 2-chloro-4-methanesulfonyl-3-(2-methoxy)ethoxybenzoic acid, 0.3 g of potassium carbonate, 0.45 g of 1-ethyl-5-hydroxypyrazole and 0.77 g of N,N'-dicyclohexyl carbodiimide were put into 40 ml of t-amyl alcohol, and the mixture was stirred under heating at a temperature of from 80° to 90°C for from 4 to 5 hours. The solvent was distilled off, and a dilute potassium carbonate aqueous solution was added to the residue. The mixture was washed with chloroform. The aqueous layer was acidified with concentrated hydrochloric acid and extracted with chloroform. The extract was dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain a crude product of the above identified compound. The crude product was recrystallized from ethanol to obtain 0.3 g of the desired product. Melting point: 159°-160°C

EXAMPLE 2
PAC Preparation of 4-(3-benzyloxy-2-chloro-4-methanesulfonylbenzoyl)-1-ethyl-5-hydroxypyrazol e (1}Benzyl 3-benzyloxy-2-chloro-4-methanesulfonylbenzoate

1.5 g of 2-chloro-3-hydroxy-4-methanesulfonylbenzoic acid, 1.7 g of potassium carbonate and 5.1 g of benzyl bromide were put into 50 ml of dimethylformamide, and the mixture was stirred at room temperature overnight and then heated at a temperature of from 60° to 70°C for 3 hours. The solvent was distilled off, and water was added to the residue. The mixture was extracted with chloroform. The extract was dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain a crude product of the above identified compound. The crude product was recrystallized from ethanol to obtain 2.5 g of the desired product.

(2) 3-benzyloxy-2-chloro-4-methanesulfonylbenzoic acid

2.5 g of benzyl 3-benzyloxy-2-chloro-4-methanesulfonylbenzoate was put into 50 ml of ethanol, and 25 ml of an aqueous solution containing 1 g of sodium hydrochloride was added thereto. The mixture was stirred at room temperature for 30 minutes. Then, ethanol was distilled off, and water was added to the residue. The mixture was washed with chloroform. The aqueous layer was acidified with concentrated hydrochloric acid and then extracted with chloroform. The extract was dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain a crude product of the above identified compound. The crude product was washed with ethanol-isopropyl ether to obtain 1.0 g of the desired product.

(3)-4-(3-benzyloxy-2-chloro-4-methanesulfonylbenzol)-ethyl-5-hydroxypyrazol

1.0 g of 3-benzyloxy-2-chloro-4methanesulfonylbenzoic acid, 0.23 g of potassium carbonate, 0.24 g of 1-ethyl-5-hydroxy-pyrazole and 0.59 g of N,N'-dicyclohexylcarbodiimide were put into 20 ml of t-amyl alcohol, and the mixture was stirred under heating at a temperature of from 80° to 90°C for 4 hours. The solvent was distilled off, and then an aqueous potassium carbonate solution was added to the residue. The mixture was washed with chloroform. The aqueous layer was acidified with concentrated hydrochloric acid and then extracted with chloroform. The extract was dried over anhydrous sodium sulfate. Then, the solvent was distilled off to obtain a crude product of the above identified compound. The crude product was recrystallized from ethanol to obtain 0.3 g of the desired product. Melting point: 162°-165°C

The physical properties of the benzoic acids and the pyrazole derivatives prepared in accordance with the preceeding Examples will be given in Tables 1 and 2 including those of the preceeding Examples.

TABLE 1
______________________________________
##STR20##
Melting
X Y Z point (°C.)
______________________________________
Cl
##STR21## SO2 Me
102∼107
Cl OCH2 CH2 OPh
SO2 Me
147∼151
Cl
##STR22## SO2 Me
153∼157
Cl OCH2 CH2 CHCH2
SO2 Me
90∼94
Cl OCH2 CHCHMe SO2 Me
113∼118
Cl OCH2 CH2 OMe
SO2 Me
89∼92
______________________________________
TABLE 2
__________________________________________________________________________
##STR23##
Compound Melting
No. A B X Y Z Q point (°C.)
__________________________________________________________________________
1 Et H Cl
OCH2 CH2 OMe
SO2 Me
H 159∼160
2 Et H Cl
OCH2 Ph
SO2 Me
H 162∼165
3 Et H Cl
##STR24## SO2 Me
H 156∼159
4 Et H Cl
##STR25## SO2 Me
H 153∼157
5 Et H Cl
OCH2 CH2 OPh
SO2 Me
H 148∼150
6 Et H Cl
OCH2 CCH
SO2 Me
H 150.7∼152.4
7 Et H Cl
OCH2 CH2 OEt
SO2 Me
H 152.3∼154.9
8 Et H Cl
OCH2 CH2 CHCH2
SO2 Me
H 131∼134
9 Et H Cl
OCH2 CH2 SMe
SO2 Me
H Oily substance
10 Et H Cl
OCH2 CH2 SO2 Me
SO2 Me
H 206∼208
11 Et H Cl
OCH2 CH2 OPr-i
SO2 Me
H 171∼174
12 Et H Cl
##STR26## SO2 Me
H 191∼193
13 Me Me Cl
##STR27## SO2 Me
H 181∼183.5
14 Et H Cl
##STR28## SO2 Me
H 100∼101
15 Et H Cl
##STR29## SO2 Me
H 171∼173
16 Me Me Cl
##STR30## SO2 Me
H 138∼142
17 Me Me Cl
##STR31## SO2 Me
H 100.5∼101
18 Et H Cl
##STR32## SO2 Me
H 154∼158
19 Et H Cl
##STR33## SO2 Me
H 175∼179
20 i-Pr
H Cl
OCH2 CH2 OMe
SO2 Me
H 180∼183
__________________________________________________________________________

Compounds which can be prepared in the same manner as the preceding Examples will be given in Tables 3 to 8 including those of the preceding Examples. However, the present invention is not restricted to such compounds.

Various symbols used in Tables 3 to 8 have the following meanings. ##STR34##

TABLE 3
______________________________________
X Y Z Q
______________________________________
Me Y1 SO2 Me
H
Me Y2 SO2 Me
H
Me Y3 SO2 Me
H
Me Y4 SO2 Me
H
Me Y5 SO2 Me
H
Me Y6 SO2 Me
H
Me Y7 SO2 Me
H
Me OCH2 CHCH2
SO2 Me
H
Me OCHMeCHCH2 SO2 Me
H
Me OCMe2 CHCH2
SO2 Me
H
Me OCH2 CMeCH2
SO2 Me
H
Me OCH2 CHCHMe SO2 Me
H
Me OCH2 CHCMe2
SO2 Me
H
Me OCH2 CH2 CHCH2
SO2 Me
H
Me OCH2 CCH SO2 Me
H
Me OCHMeC CH SO2 Me
H
Me OCMe2 CCH SO2 Me
H
Me OCH2 CCMe SO2 Me
H
Me OCH2 CH2 F
SO2 Me
H
Me OCH2 CHF2
SO2 Me
H
Me OCH2 CF3 SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CCl3
SO2 Me
H
Me OCHMeCH2 Cl SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CH2 Br
SO2 Me
H
Me Y8 SO2 Me
H
Me OCH2 CClCH2
SO2 Me
H
Me OCH2 CClCHCl SO2 Me
H
Me OCH2 CH2 NO2
SO2 Me
H
Me OPh SO2 Me
H
Me OPhMe-2 SO2 Me
H
Me OPhCl-4 SO2 Me
H
Me OPhNO2 -4 SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OEt
SO2 Me
H
Me OCH2 CH2 OPr-n
SO2 Me
H
Me OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OBu-n
SO2 Me
H
Me OCH2 CH2 OBu-i
SO2 Me
H
Me OCH2 CH2 OBu-s
SO2 Me
H
Me OCH2 CH2 OBu-t
SO2 Me
H
Me OCH2 CH2Y4
SO2 Me
H
Me OCHMeCH2 OMe SO2 Me
H
Me OCH2 CHMeOMe SO2 Me
H
Me OCH2 CH2 OPh
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Me OCH2 CH2 OH
SO2 Me
H
Me OCH2 Ph SO2 Me
H
Me OCHMePh SO2 Me
H
Me OCH2 CH2 Ph
SO2 Me
H
Me OCH2 Ph-2-Cl SO2 Me
H
Me OCH2 Ph-3-Me SO2 Me
H
Me OCH2 Ph-4-OMe SO2 Me
H
Me OCH2 Ph-4-NO2
SO2 Me
H
Me Y9 SO2 Me
H
Me Y10 SO2 Me
H
Me Y11 SO2 Me
H
Me Y12 SO2 Me
H
Me Y13 SO2 Me
H
Me Y14 SO2 Me
H
Me Y15 SO2 Me
H
Me Y16 SO2 Me
H
Me Y17 SO2 Me
H
Me Y18 SO2 Me
H
Me OCH2 CH2 NH2
SO2 Me
H
Me OCH2 CH2 NHMe
SO2 Me
H
Me OCH2 CH2 NHPr-i
SO2 Me
H
Me OCH2 CH2 NME2
SO2 Me
H
Me OCH2 CH2 NEt2
SO2 Me
H
Me Y19 SO2 Me
H
Me OCH2 COOMe SO2 Me
H
Me OCH2 COOEt SO2 Me
H
Me OCH2 COOPr-i SO2 Me
H
Me OCH2 COOBu-i SO2 Me
H
Me OCH2 COOBu-t SO2 Me
H
Me OCH2 COOY4 SO2 Me
H
Me OCHMeCOOMe SO2 Me
H
Me OCHMeCOOEt SO2 Me
H
Me OCHMeCOOPr-i SO2 Me
H
Me OCH2 CH2 CN
SO2 Me
H
Me OCH2 SMe SO 2 Me
H
Me OCH2 CH2 SMe
SO2 Me
H
Me OCH2 CH2 S(O)Me
SO2 Me
H
Me OCH2 CH2 SO2 Me
SO2 Me
H
Me OCH2 CH2 SPr-i
SO2 Me
H
Me OCH2 CH2 S(O)Pr-i
SO2 Me
H
Me OCH2 CH2 SO2 Pr-i
SO2 Me
H
Me OCOOMe SO2 Me
H
Me OCOOPr-i SO2 Me
H
Me OCONH2 SO2 Me
H
Me OCONHMe SO2 Me
H
Me OCONMe2 SO2 Me
H
Me OP(O)(OMe)2 SO2 Me
H
Me Y20 SO2 Me
H
Me SCH2 CHCH2
SO2 Me
H
Me SCH2 CHCMe2
SO2 Me
H
Me SCH2 CCH SO2 Me
H
Me SCH2 CF3 SO2 Me
H
Me SCH2 CCl3
SO2 Me
H
Me Y21 SO2 Me
H
Me SPh SO2 Me
H
Me SCH2 CH2 OMe
SO2 Me
H
Me SCH2 CH2 OEt
SO2 Me
H
Me SCH2 CH2 OPr-i
SO2 Me
H
Me Y22 SO2 Me
H
Me S(O)CH2 CHCH2
SO2 Me
H
Me S(O)CH2 CHCMe2
SO2 Me
H
Me S(O)CH2 CCH SO2 Me
H
Me S(O)CH2 CH2 Cl
SO2 Me
H
Me Y23 SO2 Me
H
Me SO2 CH2 CHCH2
SO2 Me
H
Me SO2 CH2 CHCMe2
SO2 Me
H
Me SO2 CH2 CCH
SO2 Me
H
Me SO2 CH2 CF3
SO2 Me
H
Me SO2 CH2 CH2 Cl
SO2 Me
H
Me Y24 SO2 Me
H
Me Y25 SO2 Me
H
Me SO2 Ph SO2 Me
H
Me SO2 CH2 CH2 OMe
SO2 Me
H
Me SO2 CH2 CH2 OEt
SO2 Me
H
Me SO2 CH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
CH 2 Ph
Me OCH2 CH2 OEt
SO2 Me
CH2 Ph
Me OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCHMeCH2 OMe SO2 Me
CH2 Ph
Me OCH2 CH2 SMe
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Me SCH2 CH2 OMe
SO2 Me
CH2 Ph
Me SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Me SO2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 OMe
SO2 Me
CH2 COPh
Me OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SMe
SO2 Me
CH2 COPh
Me OCH 2 CH2 SOMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Me OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Me SCH2 CH2 OMe
SO2 Me
CH2 COPh
Me SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 OMe
Cl H
Me OCH2 CH2 OEt
Cl H
Me OCH2 CH2 OPr-i
Cl H
Me OCHMeCH2 OMe Cl H
Me OCH2 COOMe Cl H
Me OCH2 CH2 SMe
Cl H
Me OCH2 CH2 SO2 Me
Cl H
Me SCH2 CH2 OMe
Cl H
Me SO2 CH2 CH2 OMe
Cl H
Me OCH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 SMe
Cl CH2 Ph
Me OCH2 CH2 SOMe
Cl CH2 Ph
Me OCH2 CH2 SO2 Me
Cl CH2 Ph
Me SCH2 CH2 OMe
Cl CH2 Ph
Me SO2 CH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 OMe
Cl CH2 COPh
Me OCH2 CH2 SMe
Cl CH2 COPh
Me OCH2 CH2 SO2 Me
Cl CH2 COPh
Me SCH2 CH2 OMe
Cl CH2 COPh
Me SCH2 CH2 OEt
Cl CH2 COPh
Me SO2 CH2 CH2 OMe
Cl CH2 COPh
Cl Y1 SO2 Me
H
Cl Y2 SO2 Me
H
Cl Y3 SO2 Me
H
Cl Y4 SO2 Me
H
Cl Y5 SO2 Me
H
Cl Y6 SO2 Me
H
Cl Y7 SO2 Me
H
Cl OCH2 CHCH2
SO2 Me
H
Cl OCHMeCHCH2 SO2 Me
H
Cl OCMe2 CHCH2
SO2 Me
H
Cl OCH2 CMeCH2
SO2 Me
H
Cl OCH2 CHCHMe SO2 Me
H
Cl OCH2 CHCMe2
SO2 Me
H
Cl OCH2 CH2 CHCH2
SO2 Me
H
Cl OCH2 CCH SO2 Me
H
Cl OCHMeCCH SO2 Me
H
Cl OCMe2 CCH SO2 Me
H
Cl OCH2 CCMe SO2 Me
H
Cl OCH2 CH2 F
SO2 Me
H
Cl OCH2 CHF2
SO2 Me
H
Cl OCH2 CF3 SO2 Me
H
Cl OCH2 CH2 Cl
SO2 Me
H
Cl OCH2 CCl3
SO2 Me
H
Cl OCHMeCH2 Cl SO2 Me
H
Cl OCH2 CH2 CH2 Cl
SO2 Me
H
Cl OCH2 CH2 Br
SO2 Me
H
Cl Y8 SO2 Me
H
Cl OCH2 CClCH2
SO2 Me
H
Cl OCH2 CClCHCl SO2 Me
H
Cl OCH2 CH2 NO2
SO2 Me
H
Cl OPh SO2 Me
H
Cl OPhMe-2 SO2 Me
H
Cl OPhCl-4 SO2 Me
H
Cl OPhNO2 -4 SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OEt
SO2 Me
H
Cl OCH2 CH2 OPr-n
SO2 Me
H
Cl OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OBu-n
SO2 Me
H
Cl OCH2 CH2 OBu-i
SO2 Me
H
Cl OCH2 CH2 OBu-s
SO2 Me
H
Cl OCH2 CH2 OBu-t
SO2 Me
H
Cl OCH2 CH2Y4
SO2 Me
H
Cl OCHMeCH2 OMe SO2 Me
H
Cl OCH2 CHMeOMe SO2 Me
H
Cl OCH2 CH2 OPh
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Cl OCH2 CH2 OH
SO2 Me
H
Cl OCH2 Ph SO2 Me
H
Cl OCHMePh SO2 Me
H
Cl OCH2 CH2 Ph
SO2 Me
H
Cl OCH2 Ph-2-Cl SO2 Me
H
Cl OCH2 Ph-3-Me SO2 Me
H
Cl OCH2 Ph-4-OMe SO2 Me
H
Cl OCH2 Ph-4-NO2
SO2 Me
H
Cl Y9 SO2 Me
H
Cl Y10 SO2 Me
H
Cl Y11 SO2 Me
H
Cl Y12 SO2 Me
H
Cl Y13 SO2 Me
H
Cl Y14 SO2 Me
H
Cl Y15 SO2 Me
H
Cl Y16 SO2 Me
H
Cl Y17 SO2 Me
H
Cl Y18 SO2 Me
H
Cl OCH2 CH2 NH2
SO2 Me
H
Cl OCH2 CH2 NHMe
SO2 Me
H
Cl OCH2 CH2 NHPr-i
SO2 Me
H
Cl OCH2 CH2 NMe2
SO2 Me
H
Cl OCH2 CH2 NEt2
SO2 Me
H
Cl Y19 SO2 Me
H
Cl OCH2 COOMe SO2 Me
H
Cl OCH2 COOEt SO2 Me
H
Cl OCH2 COOPr-i SO2 Me
H
Cl OCH2 COOBu-i SO2 Me
H
Cl OCH2 COOBu-t SO2 Me
H
Cl OCH2 COOY4 SO2 Me
H
Cl OCHMeCOOMe SO2 Me
H
Cl OCHMeCOOEt SO2 Me
H
Cl OCHMeCOOPr-i SO2 Me
H
Cl OCH2 CH2 CN
SO2 Me
H
Cl OCH2 SMe SO2 Me
H
Cl OCH2 CH2 SMe
SO2 Me
H
Cl OCH2 CH2 S(O)Me
SO2 Me
H
Cl OCH2 CH2 SO2 Me
SO2 Me
H
Cl OCH2 CH2 SPr-i
SO2 Me
H
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
H
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
H
Cl OCOOMe SO2 Me
H
Cl OCOOPr-i SO2 Me
H
Cl OCONH2 SO2 Me
H
Cl OCONHMe SO2 Me
H
Cl OCONMe2 SO2 Me
H
Cl OP(O)(OMe)2 SO2 Me
H
Cl Y20 SO2 Me
H
Cl SCH2 CHCH2
SO2 Me
H
Cl SCH2 CHCMe2
SO2 Me
H
Cl SCH2 CCH SO2 Me
H
Cl SCH2 CF3 SO2 Me
H
Cl SCH2 CCl3
SO2 Me
H
Cl Y21 SO2 Me
H
Cl SPh SO2 Me
H
Cl SCH2 CH2 OMe
SO2 Me
H
Cl SCH2 CH2 OEt
SO2 Me
H
Cl SCH2 CH2 OPr-i
SO2 Me
H
Cl Y22 SO2 Me
H
Cl S(O)CH2 CHCH2
SO2 Me
H
Cl S(O)CH2 CHCMe2
SO2 Me
H
Cl S(O)CH2 CCH SO2 Me
H
Cl S(O)CH2 CH2 Cl
SO2 Me
H
Cl Y23 SO2 Me
H
Cl SO2 CH2 CHCH2
SO2 Me
H
Cl SO2 CH2 CHCMe2
SO2 Me
H
Cl SO2 CH2 CCH
SO2 Me
H
Cl SO2 CH2 CF3
SO2 Me
H
Cl SO2 CH2 CH2 Cl
SO2 Me
H
Cl Y24 SO2 Me
H
Cl Y25 SO2 Me
H
Cl SO 2 Ph SO2 Me
H
Cl SO2 CH2 CH2 OMe
SO2 Me
H
Cl SO2 CH2 CH2 OEt
SO2 Me
H
Cl SO2 CH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 OEt
SO2 Me
CH2 Ph
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCHMeCH2 OMe SO2 Me
CH2 Ph
Cl OCH2 CH2 SMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Cl SCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OMe
SO2 Me
CH 2 Ph
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Cl SCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 OMe
Cl H
Cl OCH2 CH2 OEt
Cl H
Cl OCH2 CH2 OPr-i
Cl H
Cl OCHMeCH2 OMe Cl H
Cl OCH2 COOMe Cl H
Cl OCH2 CH2 SMe
Cl H
Cl OCH2 CH2 SO2 Me
Cl H
Cl SCH2 CH2 OMe
Cl H
Cl SO2 CH2 CH2 OMe
Cl H
Cl OCH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 SMe
Cl CH2 Ph
Cl OCH2 CH2 SOMe
Cl CH2 Ph
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 Ph
Cl SO2 CH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 OMe
Cl CH2 COPh
Cl OCH2 CH2 SMe
Cl CH2 COPh
Cl OCH2 CH2 SO2 Me
Cl CH2 COPh
Cl SCH2 CH2 OMe
Cl CH2 COPh
Cl SCH2 CH2 OEt
Cl CH2 COPh
Cl SO2 CH2 CH2 OMe
Cl CH2 COPh
OMe Y1 SO2 Me
H
OMe Y2 SO2 Me
H
OMe Y3 SO2 Me
H
OMe Y4 SO2 Me
H
OMe Y5 SO2 Me
H
OMe Y6 SO2 Me
H
OMe Y7 SO2 Me
H
OMe OCH 2 CHCH2
SO2 Me
H
OMe OCHMeCHCH2 SO2 Me
H
OMe OCMe2 CHCH2
SO2 Me
H
OMe OCH2 CMeCH2
SO2 Me
H
OMe OCH2 CHCHMe SO2 Me
H
OMe OCH2 CHCMe2
SO2 Me
H
OMe OCH2 CH2 CHCH2
SO2 Me
H
OMe OCH2 CCH SO2 Me
H
OMe OCHMeCCH SO2 Me
H
OMe OCMe2 CCH SO2 Me
H
OMe OCH2 CCMe SO2 Me
H
OMe OCH2 CH2 F
SO2 Me
H
OMe OCH2 CHF2
SO2 Me
H
OMe OCH2 CF3 SO2 Me
H
OMe OCH2 CH2 Cl
SO2 Me
H
OMe OCH2 CCl3
SO2 Me
H
OMe OCHMeCH2 Cl SO2 Me
H
OMe OCH2 CH2 CH2 Cl
SO2 Me
H
OMe OCH2 CH2 Br
SO2 Me
H
OMe Y8 SO2 Me
H
OMe OCH2 CClCH2
SO2 Me
H
OMe OCH2 CClCHCl SO2 Me
H
OMe OCH2 CH2 NO2
SO2 Me
H
OMe OPh SO2 Me
H
OMe OPhMe-2 SO2 Me
H
OMe OPhCl-4 SO2 Me
H
OMe OPhNO2 -4 SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OEt
SO2 Me
H
OMe OCH2 CH2 OPr-n
SO2 Me
H
OMe OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OBu-n
SO2 Me
H
OMe OCH2 CH2 OBu-i
SO2 Me
H
OMe OCH2 CH2 OBu-s
SO2 Me
H
OMe OCH2 CH2 OBu-t
SO2 Me
H
OMe OCH2 CH2 -Y4
SO2 Me
H
OMe OCHMeCH2 OMe SO2 Me
H
OMe OCH2 CHMeOMe SO2 Me
H
OMe OCH2 CH2 OPh
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
OMe OCH2 CH2 OH
SO2 Me
H
OMe OCH2 Ph SO2 Me
H
OMe OCHMePh SO2 Me
H
OMe OCH2 CH2 Ph
SO2 Me
H
OMe OCH2 Ph-2-Cl SO2 Me
H
OMe OCH2 Ph-3-Me SO2 Me
H
OMe OCH2 Ph-4-OMe SO2 Me
H
OMe OCH2 Ph-4-NO2
SO2 Me
H
OMe Y9 SO2 Me
H
OMe Y10 SO2 Me
H
OMe Y11 SO2 Me
H
OMe Y12 SO2 Me
H
OMe Y13 SO2 Me
H
OMe Y14 SO2 Me
H
OMe Y15 SO2 Me
H
OMe Y16 SO2 Me
H
OMe Y17 SO2 Me
H
OMe Y18 SO2 Me
H
OMe OCH2 CH2 NH2
SO2 Me
H
OMe OCH2 CH2 NHMe
SO2 Me
H
OMe OCH2 CH2 NHPr-i
SO2 Me
H
OMe OCH2 CH2 NMe2
SO2 Me
H
OMe OCH2 CH2 NEt2
SO2 Me
H
OMe Y19 SO2 Me
H
OMe OCH2 COOMe SO2 Me
H
OMe OCH2 COOEt SO2 Me
H
OMe OCH2 COOPr-i SO2 Me
H
OMe OCH2 COOBu-i SO2 Me
H
OMe OCH2 COOBu-t SO2 Me
H
OMe OCH2 COO-Y4 SO2 Me
H
OMe OCHMeCOOMe SO2 Me
H
OMe OCHMeCOOEt SO2 Me
H
OMe OCHMeCOOPr-i SO2 Me
H
OMe OCH2 CH2 CN
SO2 Me
H
OMe OCH2 SMe SO2 Me
H
OMe OCH2 CH2 SMe
SO2 Me
H
OMe OCH2 CH2 S(O)Me
SO2 Me
H
OMe OCH2 CH2 SO2 Me
SO2 Me
H
OMe OCH2 CH2 SPr-i
SO2 Me
H
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
H
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
H
OMe OCOOMe SO2 Me
H
OMe OCOOPr-i SO2 Me
H
OMe OCONH2 SO2 Me
H
OMe OCONHMe SO2 Me
H
OMe OCONMe2 SO2 Me
H
OMe OP(O)(OMe)2 SO2 Me
H
OMe Y20 SO2 Me
H
OMe SCH2 CHCH2
SO2 Me
H
OMe SCH2 CHCMe2
SO2 Me
H
OMe SCH2 CCH SO2 Me
H
OMe SCH2 CF3 SO2 Me
H
OMe SCH2 CCl3
SO2 Me
H
OMe Y21 SO2 Me
H
OMe SPh SO2 Me
H
OMe SCH2 CH2 OMe
SO2 Me
H
OMe SCH2 CH2 OEt
SO2 Me
H
OMe SCH2 CH2 OPr-i
SO2 Me
H
OMe Y22 SO2 Me
H
OMe S(O)CH2 CHCH2
SO2 Me
H
OMe S(O)CH2 CHCMe2
SO2 Me
H
OMe S(O)CH2 CCH SO2 Me
H
OMe S(O)CH2 CH2 Cl
SO2 Me
H
OMe Y23 SO2 Me
H
OMe SO2 CH2 CHCH2
SO2 Me
H
OMe SO2 CH2 CHCMe2
SO2 Me
H
OMe SO2 CH 2 CCH
SO2 Me
H
OMe SO2 CH2 CF3
SO2 Me
H
OMe SO2 CH2 CH2 Cl
SO2 Me
H
OMe Y24 SO2 Me
H
OMe Y25 SO2 Me
H
OMe SO2 Ph SO2 Me
H
OMe SO2 CH2 CH2 OMe
SO2 Me
H
OMe SO2 CH2 CH2 OEt
SO2 Me
H
OMe SO2 CH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 OEt
SO2 Me
CH2 Ph
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCHMeCH2 OMe SO2 Me
CH2 Ph
OMe OCH2 CH2 SMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
OMe SCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SOMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
OMe SCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 OMe
Cl H
OMe OCH2 CH2 OEt
Cl H
OMe OCH2 CH2 OPr-i
Cl H
OMe OCHMeCH2 OMe Cl H
OMe OCH2 COOMe Cl H
OMe OCH2 CH2 SMe
Cl H
OMe OCH2 CH2 SO2 Me
Cl H
OMe SCH2 CH2 OMe
Cl H
OMe SO2 CH2 CH2 OMe
Cl H
OMe OCH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 SMe
Cl CH2 Ph
OMe OCH2 CH2 SOMe
Cl CH2 Ph
OMe OCH2 CH2 SO2 Me
Cl CH2 Ph
OMe SCH2 CH2 OMe
Cl CH2 Ph
OMe SO2 CH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 OMe
Cl CH2 COPh
OMe OCH2 CH2 SMe
Cl CH2 COPh
OMe OCH2 CH2 SO2 Me
Cl CH2 COPh
OMe SCH2 CH2 OMe
Cl CH2 COPh
OMe SCH2 CH2 OEt
Cl CH2 COPh
OMe SO2 CH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
Y1 SO2 Me
H
CH2 OMe
Y2 SO2 Me
H
CH2 OMe
Y3 SO2 Me
H
CH2 OMe
Y4 SO2 Me
H
CH2 OMe
Y5 SO2 Me
H
CH2 OMe
Y6 SO2 Me
H
CH2 OMe
Y7 SO2 Me
H
CH2 OMe
OCH2 CHCH2
SO2 Me
H
CH2 OMe
OCHMeCHCH2 SO2 Me
H
CH2 OMe
OCMe2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CMeCH2
SO2 Me
H
CH2 OMe
OCH2 CHCHMe SO2 Me
H
CH2 OMe
OCH2 CHCMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CCH SO2 Me
H
CH2 OMe
OCHMeCCH SO2 Me
H
CH2 OMe
OCMe2 C CH SO2 Me
H
CH2 OMe
OCH2 CCMe SO2 Me
H
CH2 OMe
OCH2 CH2 F
SO2 Me
H
CH2 OMe
OCH2 CHF2
SO2 Me
H
CH2 OMe
OCH2 CF3 SO2 Me
H
CH2 OMe
OCH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CCl3
SO2 Me
H
CH2 OMe
OCHMeCH2 Cl SO2 Me
H
CH2 OMe
OCH2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CH2 Br
SO2 Me
H
CH2 OMe
Y8 SO2 Me
H
CH2 OMe
OCH2 CClCH2
SO2 Me
H
CH2 OMe
OCH2 CClCHCl SO2 Me
H
CH2 OMe
OCH2 CH2 NO2
SO2 Me
H
CH2 OMe
OPh SO2 Me
H
CH2 OMe
OPhMe-2 SO2 Me
H
CH2 OMe
OPhCl-4 SO2 Me
H
CH2 OMe
OPhNO2 -4 SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OEt
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-s
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-t
SO2 Me
H
CH2 OMe
OCH2 CH2 -Y4
SO2 Me
H
CH2 OMe
OCHMeCH2 OMe SO2 Me
H
CH2 OMe
OCH2 CHMeOMe SO2 Me
H
CH2 OMe
OCH2 CH2 OPh
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OH
SO2 Me
H
CH2 OMe
OCH2 Ph SO2 Me
H
CH2 OMe
OCHMePh SO2 Me
H
CH2 OMe
OCH2 CH2 Ph
SO2 Me
H
CH2 OMe
OCH2 Ph-2-Cl SO2 Me
H
CH2 OMe
OCH2 Ph-3-Me SO2 Me
H
CH2 OMe
OCH2 Ph-4-OMe SO2 Me
H
CH2 OMe
OCH2 Ph-4-NO2
SO2 Me
H
CH2 OMe
Y9 SO2 Me
H
CH2 OMe
Y10 SO2 Me
H
CH2 OMe
Y11 SO2 Me
H
CH2 OMe
Y12 SO2 Me
H
CH2 OMe
Y13 SO2 Me
H
CH2 OMe
Y14 SO2 Me
H
CH2 OMe
Y15 SO2 Me
H
CH2 OMe
Y16 SO2 Me
H
CH2 OMe
Y17 SO2 Me
H
CH2 OMe
Y18 SO2 Me
H
CH2 OMe
OCH2 CH2 NH2
SO2 Me
H
CH2 OMe
OCH2 CH2 NHMe
SO2 Me
H
CH2 OMe
OCH2 CH2 NHPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 NMe2
SO2 Me
H
CH 2 OMe
OCH2 CH2 NEt2
SO2 Me
H
CH2 OMe
Y19 SO2 Me
H
CH2 OMe
OCH2 COOMe SO2 Me
H
CH2 OMe
OCH2 COOEt SO2 Me
H
CH2 OMe
OCH2 COOPr-i SO2 Me
H
CH2 OMe
OCH2 COOBu-i SO2 Me
H
CH2 OMe
OCH2 COOBu-t SO2 Me
H
CH2 OMe
OCH2 COO-Y4 SO2 Me
H
CH2 OMe
OCHMeCOOMe SO2 Me
H
CH2 OMe
OCHMeCOOEt SO2 Me
H
CH2 OMe
OCHMeCOOPr-i SO2 Me
H
CH2 OMe
OCH2 CH2 CN
SO2 Me
H
CH2 OMe
OCH2 SMe SO2 Me
H
CH2 OMe
OCH2 CH2 SMe
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
H
CH2 OMe
OCOOMe SO2 Me
H
CH2 OMe
OCOOPr-i SO2 Me
H
CH2 OMe
OCONH2 SO2 Me
H
CH2 OMe
OCONHMe SO2 Me
H
CH2 OMe
OCONMe2 SO2 Me
H
CH2 OMe
OP(O)(OMe)2 SO2 Me
H
CH2 OMe
Y20 SO2 Me
H
CH2 OMe
SCH2 CHCH2
SO2 Me
H
CH2 OMe
SCH2 CHCMe2
SO2 Me
H
CH2 OMe
SCH2 CCH SO2 Me
H
CH2 OMe
SCH2 CF3 SO2 Me
H
CH2 OMe
SCH2 CCl3
SO2 Me
H
CH2 OMe
Y21 SO2 Me
H
CH2 OMe
SPh SO2 Me
H
CH2 OMe
SCH2 CH2 OMe
SO2 Me
H
CH2 OMe
SCH2 CH2 OEt
SO2 Me
H
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
Y22 SO2 Me
H
CH2 OMe
S(O)CH2 CHCH2
SO2 Me
H
CH 2 OMe
S(O)CH2 CHCMe2
SO2 Me
H
CH2 OMe
S(O)CH2 CCH SO2 Me
H
CH2 OMe
S(O)CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y23 SO2 Me
H
CH2 OMe
SO2 CH2 CHCH2
SO2 Me
H
CH2 OMe
SO2 CH2 CHCMe2
SO2 Me
H
CH2 OMe
SO2 CH2 CCH
SO2 Me
H
CH2 OMe
SO2 CH2 CF3
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y24 SO2 Me
H
CH2 OMe
SO2 Ph SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OEt
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH 2 Ph
CH2 OMe
OCH2 CH2 OEt
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCHMeCH2 OMe SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SOMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OEt
Cl H
CH2 OMe
OCH2 CH2 OPr-i
Cl H
CH2 OMe
OCHMeCH2 OMe Cl H
CH2 OMe
OCH2 COOMe Cl H
CH2 OMe
OCH2 CH2 SMe
Cl H
CH2 OMe
OCH2 CH2 SO2 Me
Cl H
CH2 OMe
SCH2 CH2 OMe
Cl H
CH2 OMe
SO2 CH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SOMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 Ph
CH2 OMe
SCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OEt
Cl CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 COPh
______________________________________
TABLE 4
______________________________________
; -
##STR35##
X Y Z Q
______________________________________
Me Y1 SO2 Me
H
Me Y2 SO2 Me
H
Me Y3 SO2 Me
H
Me Y4 SO2 Me
H
Me Y5 SO2 Me
H
Me Y6 SO2 Me
H
Me Y7 SO2 Me
H
Me OCH2 CHCH2
SO2 Me
H
Me OCHMeCHCH2 SO2 Me
H
Me OCMe2 CHCH2
SO2 Me
H
Me OCH2 CMeCH2
SO2 Me
H
Me OCH2 CHCHMe SO2 Me
H
Me OCH2 CHCMe2
SO2 Me
H
Me OCH2 CH2 CHCH2
SO2 Me
H
Me OCH2 CCH SO2 Me
H
Me OCHMeC CH SO2 Me
H
Me OCMe2 CCH SO2 Me
H
Me OCH2 CCMe SO2 Me
H
Me OCH2 CH2 F
SO2 Me
H
Me OCH2 CHF2
SO2 Me
H
Me OCH2 CF3 SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CCl3
SO2 Me
H
Me OCHMeCH2 Cl SO2 Me
H
Me OCH2 CH2 CH2 Cl
SO2 Me
H
Me OCH2 CH2 Br
SO2 Me
H
Me Y8 SO2 Me
H
Me OCH2 CClCH2
SO2 Me
H
Me OCH2 CClCHCl SO2 Me
H
Me OCH2 CH2 NO2
SO2 Me
H
Me OPh SO2 Me
H
Me OPhMe-2 SO2 Me
H
Me OPhCl-4 SO2 Me
H
Me OPhNO2 -4 SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OEt
SO2 Me
H
Me OCH2 CH2 OPr-n
SO2 Me
H
Me OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OBu-n
SO2 Me
H
Me OCH2 CH2 OBu-i
SO2 Me
H
Me OCH2 CH2 OBu-s
SO2 Me
H
Me OCH2 CH2 OBu-t
SO2 Me
H
Me OCH2 CH2Y4
SO2 Me
H
Me OCHMeCH2 OMe SO2 Me
H
Me OCH2 CHMeOMe SO2 Me
H
Me OCH2 CH2 OPh
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Me OCH2 CH2 OH
SO2 Me
H
Me OCH2 Ph SO2 Me
H
Me OCHMePh SO2 Me
H
Me OCH2 CH2 Ph
SO2 Me
H
Me OCH2 Ph-2-Cl SO2 Me
H
Me OCH2 Ph-3-Me SO2 Me
H
Me OCH2 Ph-4-OMe SO2 Me
H
Me OCH2 Ph-4-NO2
SO2 Me
H
Me Y9 SO2 Me
H
Me Y10 SO2 Me
H
Me Y11 SO2 Me
H
Me Y12 SO2 Me
H
Me Y13 SO2 Me
H
Me Y14 SO2 Me
H
Me Y15 SO2 Me
H
Me Y16 SO2 Me
H
Me Y17 SO2 Me
H
Me Y18 SO2 Me
H
Me OCH2 CH2 NH2
SO2 Me
H
Me OCH2 CH2 NHMe
SO2 Me
H
Me OCH2 CH2 NHPr-i
SO2 Me
H
Me OCH2 CH2 NMe2
SO2 Me
H
Me OCH2 CH2 NEt2
SO2 Me
H
Me Y19 SO2 Me
H
Me OCH2 COOMe SO2 Me
H
Me OCH2 COOEt SO2 Me
H
Me OCH2 COOPr-i SO2 Me
H
Me OCH2 COOBu-i SO2 Me
H
Me OCH2 COOBu-t SO2 Me
H
Me OCH2 COOY4 SO2 Me
H
Me OCHMeCOOMe SO2 Me
H
Me OCHMeCOOEt SO2 Me
H
Me OCHMeCOOPr-i SO2 Me
H
Me OCH2 CH2 CN
SO2 Me
H
Me OCH2 SMe SO2 Me
H
Me OCH2 CH2 SMe
SO2 Me
H
Me OCH2 CH2 S(O)Me
SO2 Me
H
Me OCH2 CH2 SO2 Me
SO2 Me
H
Me OCH2 CH2 SPr-i
SO2 Me
H
Me OCH2 CH2 S(O)Pr-i
SO2 Me
H
Me OCH2 CH2 SO2 Pr-i
SO2 Me
H
Me OCOOMe SO2 Me
H
Me OCOOPr-i SO2 Me
H
Me OCONH2 SO2 Me
H
Me OCONHMe SO2 Me
H
Me OCONMe2 SO2 Me
H
Me OP(O)(OMe)2 SO2 Me
H
Me Y20 SO2 Me
H
Me SCH2 CHCH2
SO2 Me
H
Me SCH2 CHCMe2
SO2 Me
H
Me SCH2 CCH SO2 Me
H
Me SCH2 CF3 SO2 Me
H
Me SCH2 CCl3
SO2 Me
H
Me Y21 SO2 Me
H
Me SPh SO2 Me
H
Me SCH2 CH2 OMe
SO2 Me
H
Me SCH2 CH2 OEt
SO2 Me
H
Me SCH2 CH2 OPr-i
SO2 Me
H
Me Y22 SO2 Me
H
Me S(O)CH2 CHCH2
SO2 Me
H
Me S(O)CH2 CHCMe2
SO2 Me
H
Me S(O)CH2 CCH SO2 Me
H
Me S(O)CH2 CH2 Cl
SO2 Me
H
Me Y23 SO2 Me
H
Me SO2 CH2 CHCH2
SO2 Me
H
Me SO2 CH2 CHCMe2
SO2 Me
H
Me SO2 CH2 CCH
SO2 Me
H
Me SO2 CH2 CF3
SO2 Me
H
Me SO2 CH2 CH2 Cl
SO2 Me
H
Me Y24 SO2 Me
H
Me Y25 SO2 Me
H
Me SO2 Ph SO2 Me
H
Me SO2 CH2 CH2 OMe
SO2 Me
H
Me SO2 CH2 CH2 OEt
SO2 Me
H
Me SO2 CH2 CH2 OPr-i
SO 2 Me
H
Me OCH2 CH2 OMe
SO2 Me
CH2 Ph
Me OCH2 CH2 OEt
SO2 Me
CH2 Ph
Me OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCHMeCH2 OMe SO2 Me
CH2 Ph
Me OCH2 CH2 SMe
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Me SCH2 CH2 OMe
SO2 Me
CH2 Ph
Me SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 OMe
SO2 Me
CH2 COPh
Me OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Me OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Me SCH2 CH2 OMe
SO2 Me
CH2 COPh
Me SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 OMe
Cl H
Me OCH2 CH2 OEt
Cl H
Me OCH2 CH2 OPr-i
Cl H
Me OCHMeCH2 OMe Cl H
Me OCH2 COOMe Cl H
Me OCH2 CH2 SMe
Cl H
Me OCH2 CH2 SO2 Me
Cl H
Me SCH2 CH2 OMe
Cl H
Me SO2 CH2 CH2 OMe
Cl H
Me OCH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 SMe
Cl CH2 Ph
Me OCH2 CH2 SOMe
Cl CH2 Ph
Me OCH2 CH2 SO2 Me
Cl CH2 Ph
Me SCH2 CH2 OMe
Cl CH2 Ph
Me SO2 CH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 OMe
Cl CH2 COPh
Me OCH2 CH2 SMe
Cl CH2 COPh
Me OCH2 CH2 SO2 Me
Cl CH2 COPh
Me SCH2 CH2 OMe
Cl CH2 COPh
Me SCH2 CH2 OEt
Cl CH2 COPh
Me SO2 CH2 CH2 OMe
Cl CH2 COPh
Cl Y1 SO2 Me
H
Cl Y2 SO2 Me
H
Cl Y3 SO2 Me
H
Cl Y4 SO2 Me
H
Cl Y5 SO2 Me
H
Cl Y6 SO2 Me
H
Cl Y7 SO2 Me
H
Cl OCH2 CHCH2
SO2 Me
H
Cl OCHMeCHCH2 SO2 Me
H
Cl OCMe2 CHCH2
SO2 Me
H
Cl OCH2 CMeCH2
SO2 Me
H
Cl OCH2 CHCHMe SO2 Me
H
Cl OCH2 CHCMe2
SO2 Me
H
Cl OCH2 CH2 CHCH2
SO2 Me
H
Cl OCH2 CCH SO2 Me
H
Cl OCHMeCCH SO2 Me
H
Cl OCMe2 CCH SO2 Me
H
Cl OCH2 CCMe SO2 Me
H
Cl OCH2 CH2 F
SO2 Me
H
Cl OCH2 CHF2
SO2 Me
H
Cl OCH2 CF3 SO2 Me
H
Cl OCH2 CH2 Cl
SO2 Me
H
Cl OCH2 CCl3
SO2 Me
H
Cl OCHMeCH2 Cl SO2 Me
H
Cl OCH2 CH2 CH2 Cl
SO2 Me
H
Cl OCH2 CH2 Br
SO2 Me
H
Cl Y8 SO2 Me
H
Cl OCH2 CClCH2
SO2 Me
H
Cl OCH2 CClCHCl SO2 Me
H
Cl OCH 2 CH2 NO2
SO2 Me
H
Cl OPh SO2 Me
H
Cl OPhMe-2 SO2 Me
H
Cl OPhCl-4 SO2 Me
H
Cl OPhNO2 -4 SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OEt
SO2 Me
H
Cl OCH2 CH2 OPr-n
SO2 Me
H
Cl OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OBu-n
SO2 Me
H
Cl OCH2 CH2 OBu-i
SO2 Me
H
Cl OCH2 CH2 OBu-s
SO2 Me
H
Cl OCH2 CH2 OBu-t
SO2 Me
H
Cl OCH2 CH2Y4
SO2 Me
H
Cl OCHMeCH2 OMe SO2 Me
H
Cl OCH2 CHMeOMe SO2 Me
H
Cl OCH2 CH2 OPh
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Cl OCH2 CH2 OH
SO2 Me
H
Cl OCH2 Ph SO2 Me
H
Cl OCHMePh SO2 Me
H
Cl OCH2 CH2 Ph
SO2 Me
H
Cl OCH2 Ph-2-Cl SO2 Me
H
Cl OCH2 Ph-3-Me SO2 Me
H
Cl OCH2 Ph-4-OMe SO2 Me
H
Cl OCH2 Ph-4-NO2
SO2 Me
H
Cl Y9 SO2 Me
H
Cl Y10 SO2 Me
H
Cl Y11 SO2 Me
H
Cl Y12 SO2 Me
H
Cl Y13 SO2 Me
H
Cl Y14 SO2 Me
H
Cl Y15 SO2 Me
H
Cl Y16 SO2 Me
H
Cl Y17 SO2 Me
H
Cl Y18 SO2 Me
H
Cl OCH2 CH2 NH2
SO2 Me
H
Cl OCH2 CH2 NHMe
SO2 Me
H
Cl OCH2 CH2 NHPr-i
SO2 Me
H
Cl OCH2 CH2 NMe2
SO2 Me
H
Cl OCH2 CH2 NEt2
SO2 Me
H
Cl Y19 SO2 Me
H
Cl OCH2 COOMe SO2 Me
H
Cl OCH2 COOEt SO2 Me
H
Cl OCH2 COOPr-i SO2 Me
H
Cl OCH2 COOBu-i SO2 Me
H
Cl OCH2 COOBu-t SO2 Me
H
Cl OCH2 COOY4 SO2 Me
H
Cl OCHMeCOOMe SO2 Me
H
Cl OCHMeCOOEt SO2 Me
H
Cl OCHMeCOOPr-i SO2 Me
H
Cl OCH2 CH2 CN
SO2 Me
H
Cl OCH2 SMe SO2 Me
H
Cl OCH2 CH2 SMe
SO2 Me
H
Cl OCH2 CH2 S(O)Me
SO2 Me
H
Cl OCH2 CH2 SO2 Me
SO2 Me
H
Cl OCH2 CH2 SPr-i
SO2 Me
H
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
H
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
H
Cl OCOOMe SO2 Me
H
Cl OCOOPr-i SO2 Me
H
Cl OCONH2 SO2 Me
H
Cl OCONHMe SO2 Me
H
Cl OCONMe2 SO2 Me
H
Cl OP(O)(OMe)2 SO2 Me
H
Cl Y20 SO2 Me
H
Cl SCH2 CHCH2
SO2 Me
H
Cl SCH2 CHCMe2
SO2 Me
H
Cl SCH2 C CH SO2 Me
H
Cl SCH2 CF3 SO2 Me
H
Cl SCH2 CCl3
SO2 Me
H
Cl Y21 SO2 Me
H
Cl SPh SO2 Me
H
Cl SCH2 CH2 OMe
SO2 Me
H
Cl SCH2 CH2 OEt
SO2 Me
H
Cl SCH2 CH2 OPr-i
SO2 Me
H
Cl Y22 SO2 Me
H
Cl S(O)CH2 CHCH2
SO2 Me
H
Cl S(O)CH2 CHCMe2
SO2 Me
H
Cl S(O)CH2 CCH SO2 Me
H
Cl S(O)CH2 CH2 Cl
SO2 Me
H
Cl Y23 SO2 Me
H
Cl SO2 CH2 CHCH2
SO2 Me
H
Cl SO2 CH2 CHCMe2
SO2 Me
H
Cl SO2 CH2 CCH
SO2 Me
H
Cl SO2 CH2 CF3
SO2 Me
H
Cl SO2 CH2 CH2 Cl
SO2 Me
H
Cl Y24 SO2 Me
H
Cl Y25 SO2 Me
H
Cl SO2 Ph SO2 Me
H
Cl SO2 CH2 CH2 OMe
SO2 Me
H
Cl SO2 CH2 CH2 OEt
SO2 Me
H
Cl SO2 CH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 OEt
SO2 Me
CH2 Ph
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCHMeCH2 OMe SO2 Me
CH2 Ph
Cl OCH2 CH2 SMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Cl SCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Cl SCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 OMe
Cl H
Cl OCH2 CH2 OEt
Cl H
Cl OCH2 CH2 OPr-i
Cl H
Cl OCHMeCH2 OMe Cl H
Cl OCH2 COOMe Cl H
Cl OCH2 CH2 SMe
Cl H
Cl OCH2 CH2 SO2 Me
Cl H
Cl SCH2 CH2 OMe
Cl H
Cl SO2 CH2 CH2 OMe
Cl H
Cl OCH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 SMe
Cl CH2 Ph
Cl OCH2 CH2 SOMe
Cl CH2 Ph
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 Ph
Cl SO2 CH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 OMe
Cl CH2 COPh
Cl OCH2 CH2 SMe
Cl CH2 COPh
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 COPh
Cl SCH2 CH2 OEt
Cl CH2 COPh
Cl SO2 CH2 CH2 OMe
Cl CH2 COPh
OMe Y1 SO2 Me
H
OMe Y2 SO2 Me
H
OMe Y3 SO2 Me
H
OMe Y4 SO2 Me
H
OMe Y5 SO2 Me
H
OMe Y6 SO2 Me
H
OMe Y7 SO2 Me
H
OMe OCH2 CHCH2
SO2 Me
H
OMe OCHMeCHCH2 SO2 Me
H
OMe OCMe2 CHCH2
SO2 Me
H
OMe OCH2 CMeCH2
SO2 Me
H
OMe OCH2 CHCHMe SO2 Me
H
OMe OCH2 CHCMe2
SO2 Me
H
OMe OCH2 CH2 CHCH2
SO2 Me
H
OMe OCH2 CCH SO2 Me
H
OMe OCHMeCCH SO2 Me
H
OMe OCMe2 CCH SO2 Me
H
OMe OCH2 CCMe SO2 Me
H
OMe OCH2 CH2 F
SO2 Me
H
OMe OCH2 CHF2
SO2 Me
H
OMe OCH2 CF3 SO2 Me
H
OMe OCH2 CH2 Cl
SO2 Me
H
OMe OCH2 CCl3
SO2 Me
H
OMe OCHMeCH2 Cl SO2 Me
H
OMe OCH2 CH2 CH2 Cl
SO2 Me
H
OMe OCH2 CH2 Br
SO2 Me
H
OMe Y8 SO2 Me
H
OMe OCH2 CClCH2
SO2 Me
H
OMe OCH2 CClCHCl SO2 Me
H
OMe OCH2 CH2 NO2
SO2 Me
H
OMe OPh SO2 Me
H
OMe OPhMe-2 SO2 Me
H
OMe OPhCl-4 SO2 Me
H
OMe OPhNO2 -4 SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OEt
SO2 Me
H
OMe OCH2 CH2 OPr-n
SO2 Me
H
OMe OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OBu-n
SO2 Me
H
OMe OCH2 CH2 OBu-i
SO2 Me
H
OMe OCH2 CH2 OBu-s
SO2 Me
H
OMe OCH2 CH2 OBu-t
SO2 Me
H
OMe OCH2 CH2Y4
SO2 Me
H
OMe OCHMeCH2 OMe SO2 Me
H
OMe OCH2 CHMeOMe SO2 Me
H
OMe OCH2 CH2 OPh
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
OMe OCH2 CH2 OH
SO2 Me
H
OMe OCH2 Ph SO2 Me
H
OMe OCHMePh SO2 Me
H
OMe OCH2 CH2 Ph
SO2 Me
H
OMe OCH2 Ph-2-Cl SO2 Me
H
OMe OCH2 Ph-3-Me SO2 Me
H
OMe OCH2 Ph-4-OMe SO2 Me
H
OMe OCH2 Ph-4-NO2
SO2 Me
H
OMe Y9 SO2 Me
H
OMe Y10 SO2 Me
H
OMe Y11 SO2 Me
H
OMe Y12 SO2 Me
H
OMe Y13 SO2 Me
H
OMe Y14 SO2 Me
H
OMe Y15 SO2 Me
H
OMe Y16 SO2 Me
H
OMe Y17 SO2 Me
H
OMe Y18 SO2 Me
H
OMe OCH2 CH2 NH2
SO2 Me
H
OMe OCH2 CH2 NHMe
SO2 Me
H
OMe OCH2 CH2 NHPr-i
SO 2 Me
H
OMe OCH2 CH2 NMe2
SO2 Me
H
OMe OCH2 CH2 NEt2
SO2 Me
H
OMe Y19 SO2 Me
H
OMe OCH2 COOMe SO2 Me
H
OMe OCH2 COOEt SO2 Me
H
OMe OCH2 COOPr-i SO2 Me
H
OMe OCH2 COOBu-i SO2 Me
H
OMe OCH2 COOBu-t SO2 Me
H
OMe OCH2 COOY4 SO2 Me
H
OMe OCHMeCOOMe SO2 Me
H
OMe OCHMeCOOEt SO2 Me
H
OMe OCHMeCOOPr-i SO2 Me
H
OMe OCH2 CH2 CN
SO2 Me
H
OMe OCH2 SMe SO2 Me
H
OMe OCH2 CH2 SMe
SO2 Me
H
OMe OCH2 CH2 S(O)Me
SO2 Me
H
OMe OCH2 CH2 SO2 Me
SO2 Me
H
OMe OCH2 CH2 SPr-i
SO2 Me
H
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
H
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
H
OMe OCOOMe SO2 Me
H
OMe OCOOPr-i SO2 Me
H
OMe OCONH2 SO2 Me
H
OMe OCONHMe SO2 Me
H
OMe OCONMe2 SO2 Me
H
OMe OP(O)(OMe)2 SO2 Me
H
OMe Y20 SO2 Me
H
OMe SCH2 CHCH2
SO2 Me
H
OMe SCH2 CHCMe2
SO2 Me
H
OMe SCH2 CCH SO2 Me
H
OMe SCH2 CF3 SO2 Me
H
OMe SCH2 CCl3
SO2 Me
H
OMe Y21 SO2 Me
H
OMe SPh SO2 Me
H
OMe SCH2 CH2 OMe
SO2 Me
H
OMe SCH2 CH2 OEt
SO2 Me
H
OMe SCH2 CH2 OPr-i
SO2 Me
H
OMe Y22 SO2 Me
H
OMe S(O)CH2 CHCH2
SO2 Me
H
OMe S(O)CH2 CHCMe2
SO2 Me
H
OMe S(O)CH2 CCH SO2 Me
H
OMe S(O)CH2 CH2 Cl
SO2 Me
H
OMe Y23 SO2 Me
H
OMe SO2 CH2 CHCH2
SO2 Me
H
OMe SO2 CH2 CHCMe2
SO2 Me
H
OMe SO2 CH2 CCH
SO2 Me
H
OMe SO2 CH2 CF3
SO2 Me
H
OMe SO2 CH2 CH2 Cl
SO2 Me
H
OMe Y24 SO2 Me
H
OMe Y25 SO2 Me
H
OMe SO2 Ph SO2 Me
H
OMe SO2 CH2 CH2 OMe
SO2 Me
H
OMe SO2 CH2 CH2 OEt
SO2 Me
H
OMe SO2 CH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 OEt
SO2 Me
CH2 Ph
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCHMeCH2 OMe SO2 Me
CH2 Ph
OMe OCH2 CH2 SMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SPr-i
SO2 Me
CH 2 Ph
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
OMe SCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SOMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
OMe SCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 OMe
Cl H
OMe OCH2 CH2 OEt
Cl H
OMe OCH2 CH2 OPr-i
Cl H
OMe OCHMeCH2 OMe Cl H
OMe OCH2 COOMe Cl H
OMe OCH2 CH2 SMe
Cl H
OMe OCH2 CH2 SO2 Me
Cl H
OMe SCH2 CH2 OMe
Cl H
OMe SO2 CH2 CH2 OMe
Cl H
OMe OCH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 SMe
Cl CH2 Ph
OMe OCH2 CH2 SOMe
Cl CH2 Ph
OMe OCH2 CH2 SO2 Me
Cl CH2 Ph
OMe SCH2 CH2 OMe
Cl CH2 Ph
OMe SO2 CH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 OMe
Cl CH2 COPh
OMe OCH2 CH2 SMe
Cl CH2 COPh
OMe OCH2 CH2 SO2 Me
Cl CH2 COPh
OMe SCH2 CH2 OMe
Cl CH2 COPh
OMe SCH 2 CH2 OEt
Cl CH2 COPh
OMe SO2 CH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
Y1 SO2 Me
H
CH2 OMe
Y2 SO2 Me
H
CH2 OMe
Y3 SO2 Me
H
CH2 OMe
Y4 SO2 Me
H
CH2 OMe
Y5 SO2 Me
H
CH2 OMe
Y6 SO2 Me
H
CH2 OMe
Y7 SO2 Me
H
CH2 OMe
OCH2 CHCH2
SO2 Me
H
CH2 OMe
OCHMeCHCH2 SO2 Me
H
CH2 OMe
OCMe2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CMeCH2
SO2 Me
H
CH2 OMe
OCH2 CHCHMe SO2 Me
H
CH2 OMe
OCH2 CHCMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CCH SO2 Me
H
CH2 OMe
OCHMeCCH SO2 Me
H
CH2 OMe
OCMe2 CCH SO2 Me
H
CH2 OMe
OCH2 CCMe SO2 Me
H
CH2 OMe
OCH2 CH2 F
SO2 Me
H
CH2 OMe
OCH2 CHF2
SO2 Me
H
CH2 OMe
OCH2 CF3 SO2 Me
H
CH2 OMe
OCH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CCl3
SO2 Me
H
CH2 OMe
OCHMeCH2 Cl SO2 Me
H
CH2 OMe
OCH2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CH2 Br
SO2 Me
H
CH2 OMe
Y8 SO2 Me
H
CH2 OMe
OCH2 CClCH2
SO2 Me
H
CH2 OMe
OCH2 CClCHCl SO2 Me
H
CH2 OMe
OCH2 CH2 NO2
SO2 Me
H
CH2 OMe
OPh SO2 Me
H
CH2 OMe
OPhMe-2 SO2 Me
H
CH2 OMe
OPhCl-4 SO2 Me
H
CH2 OMe
OPhNO2 -4 SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OEt
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-s
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-t
SO2 Me
H
CH2 OMe
OCH2 CH2 Y4
SO2 Me
H
CH2 OMe
OCHMeCH2 OMe SO2 Me
H
CH2 OMe
OCH2 CHMeOMe SO2 Me
H
CH2 OMe
OCH2 CH2 OPh
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OH
SO2 Me
H
CH2 OMe
OCH2 Ph SO2 Me
H
CH2 OMe
OCHMePh SO2 Me
H
CH2 OMe
OCH2 CH2 Ph
SO2 Me
H
CH2 OMe
OCH2 Ph-2-Cl SO2 Me
H
CH2 OMe
OCH2 Ph-3-Me SO2 Me
H
CH2 OMe
OCH2 Ph-4-OMe SO2 Me
H
CH2 OMe
OCH2 Ph-4-NO2
SO2 Me
H
CH2 OMe
Y9 SO2 Me
H
CH2 OMe
Y10 SO2 Me
H
CH2 OMe
Y11 SO2 Me
H
CH2 OMe
Y12 SO2 Me
H
CH2 OMe
Y13 SO2 Me
H
CH2 OMe
Y14 SO2 Me
H
CH2 OMe
Y15 SO2 Me
H
CH2 OMe
Y16 SO2 Me
H
CH2 OMe
Y17 SO2 Me
H
CH2 OMe
Y18 SO2 Me
H
CH2 OMe
OCH2 CH2 NH2
SO2 Me
H
CH2 OMe
OCH2 CH2 NHMe
SO2 Me
H
CH2 OMe
OCH2 CH2 NHPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 NMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 NEt2
SO2 Me
H
CH2 OMe
Y19 SO2 Me
H
CH2 OMe
OCH2 COOMe SO2 Me
H
CH2 OMe
OCH2 COOEt SO2 Me
H
CH2 OMe
OCH2 COOPr-i SO2 Me
H
CH2 OMe
OCH2 COOBu-i SO2 Me
H
CH2 OMe
OCH2 COOBu-t SO2 Me
H
CH2 OMe
OCH2 COOY4 SO2 Me
H
CH2 OMe
OCHMeCOOMe SO2 Me
H
CH2 OMe
OCHMeCOOEt SO2 Me
H
CH2 OMe
OCHMeCOOPr-i SO2 Me
H
CH2 OMe
OCH2 CH2 CN
SO2 Me
H
CH2 OMe
OCH2 SMe SO2 Me
H
CH2 OMe
OCH2 CH2 SMe
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
H
CH2 OMe
OCOOMe SO2 Me
H
CH2 OMe
OCOOPr-i SO2 Me
H
CH2 OMe
OCONH2 SO2 Me
H
CH2 OMe
OCONHMe SO2 Me
H
CH2 OMe
OCONMe2 SO2 Me
H
CH2 OMe
OP(O)(OMe)2 SO2 Me
H
CH2 OMe
Y20 SO2 Me
H
CH2 OMe
SCH2 CHCH2
SO2 Me
H
CH2 OMe
SCH2 CHCMe2
SO2 Me
H
CH2 OMe
SCH2 CCH SO2 Me
H
CH2 OMe
SCH2 CF3 SO2 Me
H
CH2 OMe
SCH2 CCl3
SO2 Me
H
CH2 OMe
Y21 SO2 Me
H
CH2 OMe
SPh SO2 Me
H
CH2 OMe
SCH2 CH2 OMe
SO2 Me
H
CH2 OMe
SCH2 CH2 OEt
SO2 Me
H
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
Y22 SO2 Me
H
CH2 OMe
S(O)CH2 CHCH2
SO2 Me
H
CH2 OMe
S(O)CH2 CHCMe2
SO2 Me
H
CH2 OMe
S(O)CH2 CCH SO2 Me
H
CH2 OMe
S(O)CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y23 SO2 Me
H
CH2 OMe
SO2 CH2 CHCH2
SO2 Me
H
CH2 OMe
SO2 CH2 CHCMe2
SO2 Me
H
CH2 OMe
SO2 CH2 CCH
SO2 Me
H
CH2 OMe
SO2 CH2 CF3
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y24 SO2 Me
H
CH2 OMe
SO2 Ph SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OEt
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OEt
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCHMeCH2 OMe SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SOMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OEt
Cl H
CH2 OMe
OCH2 CH2 OPr-i
Cl H
CH2 OMe
OCHMeCH2 OMe Cl H
CH2 OMe
OCH2 COOMe Cl H
CH2 OMe
OCH2 CH2 SMe
Cl H
CH2 OMe
OCH2 CH2 SO2 Me
Cl H
CH2 OMe
SCH2 CH2 OMe
Cl H
CH2 OMe
SO2 CH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SOMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 Ph
CH2 OMe
SCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OEt
Cl CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 COPh
______________________________________
TABLE 5
______________________________________
##STR36##
X Y Z Q
______________________________________
Me Y1 SO2 Me
H
Me Y2 SO2 Me
H
Me Y3 SO2 Me
H
Me Y4 SO2 Me
H
Me Y5 SO2 Me
H
Me Y6 SO2 Me
H
Me Y7 SO2 Me
H
Me OCH2 CHCH2
SO2 Me
H
Me OCHMeCH CH2 SO2 Me
H
Me OCMe2 CH CH2
SO2 Me
H
Me OCH2 CMe CH2
SO2 Me
H
Me OCH2 CHCHMe SO2 Me
H
Me OCH2 CHCMe2
SO2 Me
H
Me OCH2 CH2 CH CH2
SO2 Me
H
Me OCH2 C CH SO2 Me
H
Me OCHMeC CH SO2 Me
H
Me OCHMe2 CCH SO2 Me
H
Me OCH2 CCMe SO2 Me
H
Me OCH2 CH2 F
SO2 Me
H
Me OCH2 CHF2
SO2 Me
H
Me OCH2 CF3 SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CCl3
SO2 Me
H
Me OCHMeCH2 Cl SO2 Me
H
Me OCH2 CH2 CH2 Cl
SO2 Me
H
Me OCH2 CH2 Br
SO2 Me
H
Me Y8 SO2 Me
H
Me OCH2 CCl CH2
SO2 Me
H
Me OCH2 CCl CHCl SO2 Me
H
Me OCH2 CH2 NO2
SO2 Me
H
Me OPh SO2 Me
H
Me OPhMe-2 SO2 Me
H
Me OPhCl-4 SO2 Me
H
Me OPhNO2 -4 SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OEt
SO2 Me
H
Me OCH2 CH2 OPr-n
SO2 Me
H
Me OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OBu-n
SO2 Me
H
Me OCH2 CH2 OBu-i
SO2 Me
H
Me OCH2 CH2 OBu-s
SO2 Me
H
Me OCH2 CH2 OBu-t
SO2 Me
H
Me OCH2 CH2Y4
SO2 Me
H
Me OCHMeCH2 OMe SO2 Me
H
Me OCH2 CHMeOMe SO2 Me
H
Me OCH2 CH2 OPh
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Me OCH2 CH2 OH
SO2 Me
H
Me OCH2 Ph SO2 Me
H
Me OCHMePh SO2 Me
H
Me OCH2 CH2 Ph
SO2 Me
H
Me OCH2 Ph-2-Cl SO2 Me
H
Me OCH2 Ph-3-Me SO2 Me
H
Me OCH 2 Ph-4-OMe
SO2 Me
H
Me OCH2 Ph-4-NO2
SO2 Me
H
Me Y9 SO2 Me
H
Me Y10 SO2 Me
H
Me Y11 SO2 Me
H
Me Y12 SO2 Me
H
Me Y13 SO2 Me
H
Me Y14 SO2 Me
H
Me Y15 SO2 Me
H
Me Y16 SO2 Me
H
Me Y17 SO2 Me
H
Me Y18 SO2 Me
H
Me OCH2 CH2 NH2
SO2 Me
H
Me OCH2 CH2 NHMe
SO2 Me
H
Me OCH2 CH2 NHPr-i
SO2 Me
H
Me OCH2 CH2 NMe2
SO2 Me
H
Me OCH2 CH2 NEt2
SO2 Me
H
Me Y19 SO2 Me
H
Me OCH2 COOMe SO2 Me
H
Me OCH2 COOEt SO2 Me
H
Me OCH2 COOPr-i SO2 Me
H
Me OCH2 COOBu-i SO2 Me
H
Me OCH2 COOBu-t SO2 Me
H
Me OCH2 COOY4 SO2 Me
H
Me OCHMeCOOMe SO2 Me
H
Me OCHMeCOOEt SO2 Me
H
Me OCHMeCOOPr-i SO2 Me
H
Me OCH2 CH2 CN
SO2 Me
H
Me OCH2 SMe SO2 Me
H
Me OCH2 CH2 SMe
SO2 Me
H
Me OCH2 CH2 S(O)Me
SO2 Me
H
Me OCH2 CH2 SO2 Me
SO2 Me
H
Me OCH2 CH2 SPr-i
SO2 Me
H
Me OCH2 CH2 S(O)Pr-i
SO2 Me
H
Me OCH2 CH2 SO2 Pr-i
SO2 Me
H
Me OCOOMe SO2 Me
H
Me OCOOPr-i SO2 Me
H
Me OCONH2 SO2 Me
H
Me OCONHMe SO2 Me
H
Me OCONMe2 SO2 Me
H
Me OP(O)(OMe)2 SO2 Me
H
Me Y20 SO2 Me
H
Me SCH2 CHCH2
SO2 Me
H
Me SCH2 CHCMe2
SO2 Me
H
Me SCH2 C CH SO2 Me
H
Me SCH2 CF3 SO2 Me
H
Me SCH2 CCl3
SO2 Me
H
Me Y21 SO2 Me
H
Me SPh SO2 Me
H
Me SCH2 CH2 OMe
SO2 Me
H
Me SCH2 CH2 OEt
SO2 Me
H
Me SCH2 CH2 OPr-i
SO2 Me
H
Me Y22 SO2 Me
H
Me S(O)CH2 CH CH2
SO2 Me
H
Me S(O)CH2 CH CMe2
SO2 Me
H
Me S(O)CH2 CCH SO2 Me
H
Me S(O)CH2 CH2 Cl
SO2 Me
H
Me Y23 SO2 Me
H
Me SO2 CH2 CHCH2
SO2 Me
H
Me SO2 CH2 CHCMe2
SO2 Me
H
Me SO2 CH2 C CH
SO2 Me
H
Me SO2 CH2 CF3
SO2 Me
H
Me SO2 CH2 CH2 Cl
SO2 Me
H
Me Y24 SO2 Me
H
Me Y25 SO2 Me
H
Me SO2 Ph SO2 Me
H
Me SO2 CH2 CH2 OMe
SO2 Me
H
Me SO2 CH2 CH2 OEt
SO2 Me
H
Me SO2 CH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
CH2 Ph
Me OCH2 CH2 OEt
SO2 Me
CH2 Ph
Me OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCHMeCH2 OMe SO2 Me
CH2 Ph
Me OCH2 CH2 SMe
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Me SCH2 CH2 OMe
SO2 Me
CH2 Ph
Me SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 OMe
SO2 Me
CH2 COPh
Me OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Me OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Me SCH2 CH2 OMe
SO2 Me
CH2 COPh
Me SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 OMe
Cl H
Me OCH2 CH2 OEt
Cl H
Me OCH2 CH2 OPr-i
Cl H
Me OCHMeCH2 OMe Cl H
Me OCH2 COOMe Cl H
Me OCH2 CH2 SMe
Cl H
Me OCH2 CH2 SO2 Me
Cl H
Me SCH2 CH2 OMe
Cl H
Me SO2 CH2 CH2 OMe
Cl H
Me OCH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 SMe
Cl CH2 Ph
Me OCH2 CH2 SOMe
Cl CH2 Ph
Me OCH2 CH2 SO2 Me
Cl CH2 Ph
Me SCH2 SH2 OMe
Cl CH2 Ph
Me SO2 CH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 OMe
Cl CH2 COPh
Me OCH2 CH2 SMe
Cl CH2 COPh
Me OCH2 CH2 SO2 Me
Cl CH2 COPh
Me SCH2 CH2 OMe
Cl CH2 COPh
Me SCH2 CH2 OEt
Cl CH2 COPh
Me SO2 CH2 CH2 OMe
Cl CH2 COPh
Cl Y1 SO2 Me
H
Cl Y2 SO2 Me
H
Cl Y3 SO2 Me
H
Cl Y4 SO2 Me
H
Cl Y5 SO2 Me
H
Cl Y6 SO2 Me
H
Cl Y7 SO2 Me
H
Cl OCH2 CHCH2
SO2 Me
H
Cl OCHMeCH CH2 SO2 Me
H
Cl OCMe2 CH CH2
SO2 Me
H
Cl OCH2 CMe CH2
SO2 Me
H
Cl OCH2 CHCHMe SO2 Me
H
Cl OCH2 CHCMe2
SO2 Me
H
Cl OCH2 CH2 CH CH2
SO2 Me
H
Cl OCH2 C CH SO2 Me
H
Cl OCHMeCCH SO2 Me
H
Cl OCHMe2 CCH SO2 Me
H
Cl OCH2 CCMe SO2 Me
H
Cl OCH2 CH2 F
SO2 Me
H
Cl OCH2 CHF2
SO2 Me
H
Cl OCH2 CF3 SO2 Me
H
Cl OCH2 CH2 Cl
SO2 Me
H
Cl OCH2 CCl3
SO2 Me
H
Cl OCHMeCH2 Cl SO2 Me
H
Cl OCH2 CH2 CH2 Cl
SO2 Me
H
Cl OCH2 CH2 Br
SO2 Me
H
Cl Y8 SO2 Me
H
Cl OCH2 CCl CH2
SO2 Me
H
Cl OCH2 CCl CHCl SO2 Me
H
Cl OCH2 CH2 NO2
SO2 Me
H
Cl OPh SO2 Me
H
Cl OPhMe-2 SO2 Me
H
Cl OPhCl-4 SO2 Me
H
Cl OPhNO2 -4 SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OEt
SO2 Me
H
Cl OCH2 CH2 OPr-n
SO2 Me
H
Cl OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OBu-n
SO2 Me
H
Cl OCH2 CH2 OBu-i
SO2 Me
H
Cl OCH2 CH2 OBu-s
SO2 Me
H
Cl OCH2 CH2 OBu-t
SO2 Me
H
Cl OCH2 CH2Y4
SO2 Me
H
Cl OCHMeCH2 OMe SO2 Me
H
Cl OCH2 CHMeOMe SO2 Me
H
Cl OCH2 CH2 OPh
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Cl OCH2 CH2 OH
SO2 Me
H
Cl OCH2 Ph SO2 Me
H
Cl OCHMePh SO2 Me
H
Cl OCH2 CH2 Ph
SO2 Me
H
Cl OCH2 Ph-2-Cl SO2 Me
H
Cl OCH2 Ph-3-Me SO2 Me
H
Cl OCH2 Ph-4-OMe SO2 Me
H
Cl OCH2 Ph-4-NO2
SO2 Me
H
Cl Y9 SO2 Me
H
Cl Y10 SO2 Me
H
Cl Y11 SO2 Me
H
Cl Y12 SO2 Me
H
Cl Y13 SO2 Me
H
Cl Y14 SO2 Me
H
Cl Y15 SO2 Me
H
Cl Y16 SO2 Me
H
Cl Y17 SO2 Me
H
Cl Y18 SO2 Me
H
Cl OCH2 CH2 NH2
SO2 Me
H
Cl OCH2 CH2 NHMe
SO2 Me
H
Cl OCH2 CH2 NHPr-i
SO2 Me
H
Cl OCH2 CH2 NMe2
SO2 Me
H
Cl OCH2 CH2 NEt2
SO2 Me
H
Cl Y19 SO2 Me
H
Cl OCH2 COOMe SO2 Me
H
Cl OCH2 COOEt SO2 Me
H
Cl OCH2 COOPr-i SO2 Me
H
Cl OCH2 COOBu-i SO2 Me
H
Cl OCH2 COOBu-t SO2 Me
H
Cl OCH2 COOY4 SO2 Me
H
Cl OCHMeCOOMe SO2 Me
H
Cl OCHMeCOOEt SO2 Me
H
Cl OCHMeCOOPr-i SO2 Me
H
Cl OCH2 CH2 CN
SO2 Me
H
Cl OCH2 SMe SO2 Me
H
Cl OCH2 CH2 SMe
SO2 Me
H
Cl OCH2 CH2 S(O)Me
SO2 Me
H
Cl OCH2 CH2 SO2 Me
SO2 Me
H
Cl OCH2 CH2 SPr-i
SO2 Me
H
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
H
Cl OCH2 CH2 CO2 Pr-i
SO2 Me
H
Cl OCOOMe SO2 Me
H
Cl OCOOPr-i SO2 Me
H
Cl OCONH2 SO2 Me
H
Cl OCONHMe SO2 Me
H
Cl OCONMe2 SO2 Me
H
Cl OP(O)(OMe)2 SO2 Me
H
Cl Y20 SO2 Me
H
Cl SCH2 CHCH2
SO 2 Me
H
Cl SCH2 CHCMe2
SO2 Me
H
Cl SCH2 C CH SO2 Me
H
Cl SCH2 CF3 SO2 Me
H
Cl SCH2 CCl3
SO2 Me
H
Cl Y21 SO2 Me
H
Cl SPh SO2 Me
H
Cl SCH2 CH2 OMe
SO2 Me
H
Cl SCH2 CH2 OEt
SO2 Me
H
Cl SCH2 CH2 OPr-i
SO2 Me
H
Cl Y22 SO2 Me
H
Cl S(O)CH2 CH CH2
SO2 Me
H
Cl S(O)CH2 CH CMe2
SO2 Me
H
Cl S(O)CH2 CCH SO2 Me
H
Cl S(O)CH2 CH2 Cl
SO2 Me
H
Cl Y23 SO2 Me
H
Cl SO2 CH2 CHCH2
SO2 Me
H
Cl SO2 CH2 CHCMe2
SO2 Me
H
Cl SO2 CH2 C CH
SO2 Me
H
Cl SO2 CH2 CF3
SO2 Me
H
Cl SO2 CH2 CH2 Cl
SO2 Me
H
Cl Y24 SO2 Me
H
Cl Y25 SO2 Me
H
Cl SO2 Ph SO2 Me
H
Cl SO2 CH2 CH2 OMe
SO2 Me
H
Cl SO2 CH2 CH2 OEt
SO2 Me
H
Cl SO2 CH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 OEt
SO2 Me
CH2 Ph
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCHMeCH2 OMe SO2 Me
CH2 Ph
Cl OCH2 CH2 SMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Cl SCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Cl SCH2 CH2 OMe
SO2 Cl
CH2 COPh
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 OMe
Cl H
Cl OCH2 CH2 OEt
Cl H
Cl OCH2 CH2 OPr-i
Cl H
Cl OCHMeCH2 OMe Cl H
Cl OCH2 COOMe Cl H
Cl OCH2 CH2 SMe
Cl H
Cl OCH2 CH2 SO2 Me
Cl H
Cl SCH2 CH2 OMe
Cl H
Cl SO2 CH2 CH2 OMe
Cl H
Cl OCH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 SMe
Cl CH2 Ph
Cl OCH2 CH2 SOMe
Cl CH2 Ph
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 Ph
Cl SO2 CH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 OMe
Cl CH2 COPh
Cl OCH2 CH2 SMe
Cl CH2 COPh
Cl OCH2 CH2 SO2 Me
Cl CH2 COPh
Cl SCH2 CH2 OMe
Cl CH2 COPh
Cl SCH2 CH2 OEt
Cl CH2 COPh
Cl SO2 CH2 CH2 OMe
Cl CH2 COPh
OMe Y1 SO2 Me
H
OMe Y2 SO2 Me
H
OMe Y3 SO2 Me
H
OMe Y4 SO2 Me
H
OMe Y5 SO2 Me
H
OMe Y6 SO2 Me
H
OMe Y7 SO2 Me
H
OMe OCH2 CHCH2
SO2 Me
H
OMe OCHMeCH CH2 SO2 Me
H
OMe OCMe2 CH CH2
SO2 Me
H
OMe OCH2 CMe CH2
SO2 Me
H
OMe OCH2 CHCHMe SO2 Me
H
OMe OCH2 CHCMe2
SO2 Me
H
OMe OCH2 CH2 CH CH2
SO2 Me
H
OMe OCH2 C CH SO2 Me
H
OMe OCHMeCCH SO2 Me
H
OMe OCHMe2 CCH SO2 Me
H
OMe OCH2 CCMe SO2 Me
H
OMe OCH2 CH2 F
SO2 Me
H
OMe OCH2 CHF2
SO2 Me
H
OMe OCH2 CF3 SO2 Me
H
OMe OCH2 CH2 Cl
SO2 Me
H
OMe OCH2 CCl3
SO2 Me
H
OMe OCHMeCH2 Cl SO2 Me
H
OMe OCH2 CH2 CH2 Cl
SO2 Me
H
OMe OCH2 CH2 Br
SO2 Me
H
OMe Y8 SO2 Me
H
OMe OCH2 CCl CH2
SO2 Me
H
OMe OCH2 CCl CHCl SO2 Me
H
OMe OCH2 CH2 NO2
SO2 Me
H
OMe OPh SO2 Me
H
OMe OPhMe-2 SO2 Me
H
OMe OPhCl-4 SO2 Me
H
OMe OPhNO2 -4 SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OEt
SO2 Me
H
OMe OCH2 CH2 OPr-n
SO2 Me
H
OMe OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OBu-n
SO2 Me
H
OMe OCH2 CH2 OBu-i
SO2 Me
H
OMe OCH2 CH2 OBu-s
SO2 Me
H
OMe OCH2 CH2 OBu-t
SO2 Me
H
OMe OCH2 CH2Y4
SO2 Me
H
OMe OCHMeCH2 OMe SO2 Me
H
OMe OCH2 CHMeOMe SO2 Me
H
OMe OCH2 CH2 OPh
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
OMe OCH2 CH2 OH
SO2 Me
H
OMe OCH2 Ph SO2 Me
H
OMe OCHMePh SO2 Me
H
OMe OCH2 CH2 Ph
SO2 Me
H
OMe OCH2 Ph-2-Cl SO2 Me
H
OMe OCH2 Ph-3-Me SO2 Me
H
OMe OCH2 Ph-4-OMe SO2 Me
H
OMe OCH2 Ph-4-NO2
SO2 Me
H
OMe Y9 SO2 Me
H
OMe Y10 SO2 Me
H
OMe Y11 SO2 Me
H
OMe Y12 SO2 Me
H
OMe Y13 SO2 Me
H
OMe Y14 SO2 Me
H
OMe Y15 SO2 Me
H
OMe Y16 SO2 Me
H
OMe Y17 SO2 Me
H
OMe Y18 SO2 Me
H
OMe OCH2 CH2 NH2
SO2 Me
H
OMe OCH2 CH2 NHMe
SO2 Me
H
OMe OCH2 CH2 NHPr-i
SO2 Me
H
OMe OCH2 CH2 NMe2
SO2 Me
H
OMe OCH2 CH2 NEt2
SO2 Me
H
OMe Y19 SO2 Me
H
OMe OCH2 COOMe SO2 Me
H
OMe OCH2 COOEt SO2 Me
H
OMe OCH2 COOPr-i SO2 Me
H
OMe OCH2 COOBu-i SO2 Me
H
OMe OCH2 COOBu-t SO2 Me
H
OMe OCH2 COOY4 SO2 Me
H
OMe OCHMeCOOMe SO2 Me
H
OMe OCHMeCOOEt SO2 Me
H
OMe OCHMeCOOPr-i SO2 Me
H
OMe OCH2 CH2 CN
SO2 Me
H
OMe OCH2 SMe SO2 Me
H
OMe OCH2 CH2 SMe
SO2 Me
H
OMe OCH2 CH2 S(O)Me
SO2 Me
H
OMe OCH2 CH2 SO2 Me
SO2 Me
H
OMe OCH2 CH2 SPr-i
SO2 Me
H
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
H
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
H
OMe OCOOMe SO2 Me
H
OMe OCOOPr-i SO2 Me
H
OMe OCONH2 SO2 Me
H
OMe OCONHMe SO2 Me
H
OMe OCONMe2 SO2 Me
H
OMe OP(O)(OMe)2 SO2 Me
H
OMe Y20 SO2 Me
H
OMe SCH2 CHCH2
SO2 Me
H
OMe SCH2 CHCMe2
SO2 Me
H
OMe SCH2 CCH SO2 Me
H
OMe SCH2 CF3 SO2 Me
H
OMe SCH2 CCl3
SO2 Me
H
OMe Y21 SO2 Me
H
OMe SPh SO2 Me
H
OMe SCH2 CH2 OMe
SO2 Me
H
OMe SCH2 CH2 OEt
SO2 Me
H
OMe SCH2 CH2 OPr-i
SO2 Me
H
OMe Y22 SO2 Me
H
OMe S(O)CH2 CHCH2
SO2 Me
H
OMe S(O)CH2 CHCMe2
SO2 Me
H
OMe S(O)CH2 CCH SO2 Me
H
OMe S(O)CH2 CH2 Cl
SO2 Me
H
OMe Y23 SO2 Me
H
OMe SO2 CH2 CHCH2
SO2 Me
H
OMe SO2 CH2 CHCMe2
SO2 Me
H
OMe SO2 CH2 CCH
SO2 Me
H
OMe SO2 CH2 CF3
SO2 Me
H
OMe SO2 CH2 CH2 Cl
SO2 Me
H
OMe Y24 SO2 Me
H
OMe Y25 SO2 Me
H
OMe SO2 Ph SO2 Me
H
OMe SO2 CH2 CH2 OMe
SO2 Me
H
OMe SO2 CH2 CH2 OEt
SO2 Me
H
OMe SO2 CH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 OEt
SO2 Me
CH2 Ph
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCHMeCH2 OMe SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
OMe SCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SOMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
OMe SCH2 CH2 OMe
SO2 Cl
CH2 COPh
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 OMe
Cl H
OMe OCH2 CH2 OEt
Cl H
OMe OCH2 CH2 OPr-i
Cl H
OMe OCHMeCH2 OMe Cl H
OMe OCH2 COOMe Cl H
OMe OCH2 CH2 SMe
Cl H
OMe OCH2 CH2 SO2 Me
Cl H
OMe SCH2 CH2 OMe
Cl H
OMe SO2 CH2 CH2 OMe
Cl H
OMe OCH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 SMe
Cl CH2 Ph
OMe OCH2 CH2 SOMe
Cl CH2 Ph
OMe OCH2 CH2 SO2 Me
Cl CH2 Ph
OMe SCH2 SH2 OMe
Cl CH2 Ph
OMe SO2 CH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 OMe
Cl CH2 COPh
OMe OCH2 CH2 SMe
Cl CH2 COPh
OMe OCH2 CH2 SO2 Me
Cl CH2 COPh
OMe SCH2 CH2 OMe
Cl CH2 COPh
OMe SCH2 CH2 OEt
Cl CH2 COPh
OMe SO2 CH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
Y1 SO2 Me
H
CH2 OMe
Y2 SO2 Me
H
CH2 OMe
Y3 SO2 Me
H
CH2 OMe
Y4 SO2 Me
H
CH2 OMe
Y5 SO2 Me
H
CH2 OMe
Y6 SO2 Me
H
CH2 OMe
Y7 SO2 Me
H
CH2 OMe
OCH2 CHCH2
SO2 Me
H
CH2 OMe
OCHMeCH CH2 SO2 Me
H
CH2 OMe
OCMe2 CH CH2
SO2 Me
H
CH2 OMe
OCH2 CMe CH2
SO2 Me
H
CH2 OMe
OCH2 CHCHMe SO2 Me
H
CH2 OMe
OCH2 CHCMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 CH CH2
SO2 Me
H
CH2 OMe
OCH 2 C CH SO2 Me
H
CH2 OMe
OCHMeCCH SO2 Me
H
CH2 OMe
OCHMe2 CCH SO2 Me
H
CH2 OMe
OCH2 CCMe SO2 Me
H
CH2 OMe
OCH2 CH2 F
SO2 Me
H
CH2 OMe
OCH2 CHF2
SO2 Me
H
CH2 OMe
OCH2 CF3 SO2 Me
H
CH2 OMe
OCH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CCl3
SO2 Me
H
CH2 OMe
OCHMeCH2 Cl SO2 Me
H
CH2 OMe
OCH2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CH2 Br
SO2 Me
H
CH2 OMe
Y8 SO2 Me
H
CH2 OMe
OCH2 CCl CH2
SO2 Me
H
CH2 OMe
OCH2 CCl CHCl SO2 Me
H
CH2 OMe
OCH2 CH2 NO2
SO2 Me
H
CH2 OMe
OPh SO2 Me
H
CH2 OMe
OPhMe-2 SO2 Me
H
CH2 OMe
OPhCl-4 SO2 Me
H
CH2 OMe
OPhNO2 -4 SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OEt
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-s
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-t
SO2 Me
H
CH2 OMe
OCH2 CH2Y4
SO2 Me
H
CH2 OMe
OCHMeCH2 OMe SO2 Me
H
CH2 OMe
OCH2 CHMeOMe SO2 Me
H
CH2 OMe
OCH2 CH2 OPh
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OH
SO2 Me
H
CH2 OMe
OCH2 Ph SO2 Me
H
CH2 OMe
OCHMePh SO2 Me
H
CH2 OMe
OCH2 CH2 Ph
SO2 Me
H
CH2 OMe
OCH2 Ph-2-Cl SO2 Me
H
CH2 OMe
OCH2 Ph-3-Me SO2 Me
H
CH2 OMe
OCH2 Ph-4-OMe SO2 Me
H
CH2 OMe
OCH2 Ph-4-NO2
SO2 Me
H
CH2 OMe
Y9 SO2 Me
H
CH2 OMe
Y10 SO2 Me
H
CH2 OMe
Y11 SO2 Me
H
CH2 OMe
Y12 SO2 Me
H
CH2 OMe
Y13 SO2 Me
H
CH2 OMe
Y14 SO2 Me
H
CH2 OMe
Y15 SO2 Me
H
CH2 OMe
Y16 SO2 Me
H
CH2 OMe
Y17 SO2 Me
H
CH2 OMe
Y18 SO2 Me
H
CH2 OMe
OCH2 CH2 NH2
SO2 Me
H
CH2 OMe
OCH2 CH2 NHMe
SO2 Me
H
CH2 OMe
OCH2 CH2 NHPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 NMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 NEt2
SO2 Me
H
CH2 OMe
Y19 SO2 Me
H
CH2 OMe
OCH2 COOMe SO2 Me
H
CH2 OMe
OCH2 COOEt SO2 Me
H
CH2 OMe
OCH2 COOPr-i SO2 Me
H
CH2 OMe
OCH2 COOBu-i SO2 Me
H
CH2 OMe
OCH2 COOBu-t SO2 Me
H
CH2 OMe
OCH2 COOY4 SO2 Me
H
CH2 OMe
OCHMeCOOMe SO2 Me
H
CH2 OMe
OCHMeCOOEt SO2 Me
H
CH2 OMe
OCHMeCOOPr-i SO2 Me
H
CH2 OMe
OCH2 CH2 CN
SO2 Me
H
CH2 OMe
OCH2 SMe SO2 Me
H
CH2 OMe
OCH2 CH2 SMe
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 CO2 Pr-i
SO2 Me
H
CH2 OMe
OCOOMe SO2 Me
H
CH2 OMe
OCOOPr-i SO2 Me
H
CH2 OMe
OCONH2 SO2 Me
H
CH2 OMe
OCONHMe SO2 Me
H
CH2 OMe
OCONMe2 SO2 Me
H
CH2 OMe
OP(O)(OMe)2 SO2 Me
H
CH2 OMe
Y20 SO2 Me
H
CH2 OMe
SCH2 CHCH2
SO2 Me
H
CH2 OMe
SCH2 CHCMe2
SO2 Me
H
CH2 OMe
SCH2 C CH SO2 Me
H
CH2 OMe
SCH2 CF3 SO2 Me
H
CH2 OMe
SCH2 CCl3
SO2 Me
H
CH2 OMe
Y21 SO2 Me
H
CH2 OMe
SPh SO2 Me
H
CH2 OMe
SCH 2 CH2 OMe
SO2 Me
H
CH2 OMe
SCH2 CH2 OEt
SO2 Me
H
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
Y22 SO2 Me
H
CH2 OMe
S(O)CH2 CH CH2
SO2 Me
H
CH2 OMe
S(O)CH2 CH CMe2
SO2 Me
H
CH2 OMe
S(O)CH2 CCH SO2 Me
H
CH2 OMe
S(O)CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y23 SO2 Me
H
CH2 OMe
SO2 CH2 CHCH2
SO2 Me
H
CH2 OMe
SO2 CH2 CHCMe2
SO2 Me
H
CH2 OMe
SO2 CH2 C CH
SO2 Me
H
CH2 OMe
SO2 CH2 CF3
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y24 SO2 Me
H
CH2 OMe
SO2 Ph SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OEt
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OEt
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCHMeCH2 OMe SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SOMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OMe
SO2 Cl
CH2 COPh
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH 2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OEt
Cl H
CH2 OMe
OCH2 CH2 OPr-i
Cl H
CH2 OMe
OCHMeCH2 OMe Cl H
CH2 OMe
OCH2 COOMe Cl H
CH2 OMe
OCH2 CH2 SMe
Cl H
CH2 OMe
OCH2 CH2 SO2 Me
Cl H
CH2 OMe
SCH2 CH2 OMe
Cl H
CH2 OMe
SO2 CH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SOMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 Ph
CH2 OMe
SCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OEt
Cl CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 COPh
______________________________________
TABLE 6
______________________________________
##STR37##
X Y Z Q
______________________________________
Me Y1 SO2 Me
H
Me Y2 SO2 Me
H
Me Y3 SO2 Me
H
Me Y4 SO2 Me
H
Me Y5 SO2 Me
H
Me Y6 SO2 Me
H
Me Y7 SO2 Me
H
Me OCH2 CHCH2
SO2 Me
H
Me OCHMeCHCH2 SO2 Me
H
Me OCMe2 CHCH2
SO2 Me
H
Me OCH2 CMeCH2
SO2 Me
H
Me OCH2 CHCHMe SO2 Me
H
Me OCH2 CHCMe2
SO2 Me
H
Me OCH2 CH2 CHCH2
SO2 Me
H
Me OCH2 CCH SO2 Me
H
Me OCHMeC CH SO2 Me
H
Me OCMe2 CCH SO2 Me
H
Me OCH2 CCMe SO2 Me
H
Me OCH2 CH2 F
SO2 Me
H
Me OCH2 CHF2
SO2 Me
H
Me OCH2 CF3 SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CCl3
SO2 Me
H
Me OCHMeCH2 Cl SO2 Me
H
Me OCH2 CH2 CH2 Cl
SO2 Me
H
Me OCH2 CH2 Br
SO2 Me
H
Me Y8 SO2 Me
H
Me OCH2 CClCH2
SO2 Me
H
Me OCH2 CClCHCl SO2 Me
H
Me OCH2 CH2 NO2
SO2 Me
H
Me OPh SO2 Me
H
Me OPhMe-2 SO2 Me
H
Me OPhCl-4 SO2 Me
H
Me OPhNO2 -4 SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH 2 OEt
SO2 Me
H
Me OCH2 CH2 OPr-n
SO2 Me
H
Me OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OBu-n
SO2 Me
H
Me OCH2 CH2 OBu-i
SO2 Me
H
Me OCH2 CH2 OBu-s
SO2 Me
H
Me OCH2 CH2 OBu-t
SO2 Me
H
Me OCH2 CH2Y4
SO2 Me
H
Me OCHMeCH2 OMe SO2 Me
H
Me OCH2 CHMeOMe SO2 Me
H
Me OCH2 CH2 OPh
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Me OCH2 CH2 OH
SO2 Me
H
Me OCH2 Ph SO2 Me
H
Me OCHMePh SO2 Me
H
Me OCH2 CH2 Ph
SO2 Me
H
Me OCH2 Ph-2-Cl SO2 Me
H
Me OCH2 Ph-3-Me SO2 Me
H
Me OCH2 Ph-4-OMe SO2 Me
H
Me OCH2 Ph-4-NO2
SO2 Me
H
Me Y9 SO2 Me
H
Me Y10 SO2 Me
H
Me Y11 SO2 Me
H
Me Y12 SO2 Me
H
Me Y13 SO2 Me
H
Me Y14 SO2 Me
H
Me Y15 SO2 Me
H
Me Y16 SO2 Me
H
Me Y17 SO2 Me
H
Me Y18 SO2 Me
H
Me OCH2 CH2 NH2
SO2 Me
H
Me OCH2 CH2 NHMe
SO2 Me
H
Me OCH2 CH2 NHPr-i
SO2 Me
H
Me OCH2 CH2 NMe2
SO2 Me
H
Me OCH2 CH2 NEt2
SO2 Me
H
Me Y19 SO2 Me
H
Me OCH2 COOMe SO2 Me
H
Me OCH2 COOEt SO2 Me
H
Me OCH2 COOPr-i SO2 Me
H
Me OCH2 COOBu-i SO2 Me
H
Me OCH2 COOBu-t SO2 Me
H
Me OCH2 COOY4 SO2 Me
H
Me OCHMeCOOMe SO2 Me
H
Me OCHMeCOOEt SO2 Me
H
Me OCHMeCOOPr-i SO2 Me
H
Me OCH2 CH2 CN
SO2 Me
H
Me OCH2 SMe SO2 Me
H
Me OCH2 CH2 SMe
SO2 Me
H
Me OCH2 CH2 S(O)Me
SO2 Me
H
Me OCH2 CH2 SO2 Me
SO2 Me
H
Me OCH2 CH2 SPr-i
SO2 Me
H
Me OCH2 CH2 S(O)Pr-i
SO2 Me
H
Me OCH2 CH2 SO2 Pr-i
SO2 Me
H
Me OCOOMe SO2 Me
H
Me OCOOPr-i SO2 Me
H
Me OCONH2 SO2 Me
H
Me OCONHMe SO2 Me
H
Me OCONMe2 SO2 Me
H
Me OP(O)(OMe)2 SO2 Me
H
Me Y20 SO2 Me
H
Me SCH2 CHCH2
SO2 Me
H
Me SCH2 CHCMe2
SO2 Me
H
Me SCH2 CCH SO2 Me
H
Me SCH2 CF3 SO2 Me
H
Me SCH2 CCl3
SO2 Me
H
Me Y21 SO2 Me
H
Me SPh SO2 Me
H
Me SCH2 CH2 OMe
SO2 Me
H
Me SCH2 CH2 OEt
SO2 Me
H
Me SCH2 CH2 OPr-i
SO2 Me
H
Me Y22 SO2 Me
H
Me S(O)CH2 CHCH2
SO2 Me
H
Me S(O)CH2 CHCMe2
SO2 Me
H
Me S(O)CH2 CCH SO2 Me
H
Me S(O)CH2 CH2 Cl
SO2 Me
H
Me Y23 SO2 Me
H
Me SO2 CH2 CHCH2
SO2 Me
H
Me SO2 CH2 CHCMe2
SO2 Me
H
Me SO2 CH2 CCH
SO2 Me
H
Me SO2 CH2 CF3
SO2 Me
H
Me SO2 CH2 CH2 Cl
SO2 Me
H
Me Y24 SO2 Me
H
Me Y25 SO2 Me
H
Me SO2 Ph SO2 Me
H
Me SO2 CH2 CH2 OMe
SO2 Me
H
Me SO2 CH2 CH2 OEt
SO2 Me
H
Me SO2 CH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
CH2 Ph
Me OCH2 CH2 OEt
SO2 Me
CH2 Ph
Me OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCHMeCH2 OMe SO2 Me
CH2 Ph
Me OCH2 CH2 SMe
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Me SCH2 CH2 OMe
SO2 Me
CH2 Ph
Me SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 OMe
SO2 Me
CH2 COPh
Me OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Me OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Me SCH2 CH2 OMe
SO2 Me
CH2 COPh
Me SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 OMe
Cl H
Me OCH2 CH2 OEt
Cl H
Me OCH2 CH2 OPr-i
Cl H
Me OCHMeCH2 OMe Cl H
Me OCH2 COOMe Cl H
Me OCH2 CH2 SMe
Cl H
Me OCH2 CH2 SO2 Me
Cl H
Me SCH2 CH2 OMe
Cl H
Me SO2 CH2 CH2 OMe
Cl H
Me OCH2 CH2 OMe
Cl CH2 Ph
Me OCH 2 CH2 SMe
Cl CH2 Ph
Me OCH2 CH2 SOMe
Cl CH2 Ph
Me OCH2 CH2 SO2 Me
Cl CH2 Ph
Me SCH2 CH2 OMe
Cl CH2 Ph
Me SO2 CH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 OMe
Cl CH2 COPh
Me OCH2 CH2 SMe
Cl CH2 COPh
Me OCH2 CH2 SO2 Me
Cl CH2 COPh
Me SCH2 CH2 OMe
Cl CH2 COPh
Me SCH2 CH2 OEt
Cl CH2 COPh
Me SO2 CH2 CH2 OMe
Cl CH2 COPh
Cl Y1 SO2 Me
H
Cl Y2 SO2 Me
H
Cl Y3 SO2 Me
H
Cl Y4 SO2 Me
H
Cl Y5 SO2 Me
H
Cl Y6 SO2 Me
H
Cl Y7 SO2 Me
H
Cl OCH2 CHCH2
SO2 Me
H
Cl OCHMeCHCH2 SO2 Me
H
Cl OCMe2 CHCH2
SO2 Me
H
Cl OCH2 CMeCH2
SO2 Me
H
Cl OCH2 CH CHMe SO2 Me
H
Cl OCH2 CHCMe2
SO2 Me
H
Cl OCH2 CH2 CHCH2
SO2 Me
H
Cl OCH2 CCH SO2 Me
H
Cl OCHMeCCH SO2 Me
H
Cl OCMe2 CCH SO2 Me
H
Cl OCH2 CCMe SO2 Me
H
Cl OCH2 CH2 F
SO2 Me
H
Cl OCH2 CHF2
SO2 Me
H
Cl OCH2 CF3 SO2 Me
H
Cl OCH2 CH2 Cl
SO2 Me
H
Cl OCH2 CCl3
SO2 Me
H
Cl OCHMeCH2 Cl SO2 Me
H
Cl OCH2 CH2 CH2 Cl
SO2 Me
H
Cl OCH2 CH2 Br
SO2 Me
H
Cl Y8 SO2 Me
H
Cl OCH2 CClCH2
SO2 Me
H
Cl OCH2 CClCHCl SO2 Me
H
Cl OCH2 CH2 NO2
SO2 Me
H
Cl OPh SO2 Me
H
Cl OPhMe-2 SO2 Me
H
Cl OPhCl-4 SO2 Me
H
Cl OPhNO2 -4 SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OEt
SO2 Me
H
Cl OCH2 CH2 OPr-n
SO2 Me
H
Cl OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OBu-n
SO2 Me
H
Cl OCH2 CH2 OBu-i
SO2 Me
H
Cl OCH2 CH2 OBu-s
SO2 Me
H
Cl OCH2 CH2 OBu-t
SO2 Me
H
Cl OCH2 CH2Y4
SO2 Me
H
Cl OCHMeCH2 OMe SO2 Me
H
Cl OCH2 CHMeOMe SO2 Me
H
Cl OCH2 CH2 OPh
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Cl OCH2 CH2 OH
SO2 Me
H
Cl OCH2 Ph SO2 Me
H
Cl OCHMePh SO2 Me
H
Cl OCH2 CH2 Ph
SO2 Me
H
Cl OCH2 Ph-2-Cl SO2 Me
H
Cl OCH2 Ph-3-Me SO2 Me
H
Cl OCH2 Ph-4-OMe SO2 Me
H
Cl OCH2 Ph-4-NO2
SO2 Me
H
Cl Y9 SO2 Me
H
Cl Y10 SO2 Me
H
Cl Y11 SO2 Me
H
Cl Y12 SO2 Me
H
Cl Y13 SO2 Me
H
Cl Y14 SO2 Me
H
Cl Y15 SO2 Me
H
Cl Y16 SO2 Me
H
Cl Y17 SO2 Me
H
Cl Y18 SO2 Me
H
Cl OCH2 CH2 NH2
SO2 Me
H
Cl OCH2 CH2 NHMe
SO2 Me
H
Cl OCH2 CH2 NHPr-i
SO2 Me
H
Cl OCH2 CH2 NMe2
SO2 Me
H
Cl OCH2 CH2 NEt2
SO2 Me
H
Cl Y19 SO2 Me
H
Cl OCH2 COOMe SO2 Me
H
Cl OCH2 COOEt SO2 Me
H
Cl OCH2 COOPr-i SO2 Me
H
Cl OCH2 COOBu-i SO2 Me
H
Cl OCH2 COOBu-t SO2 Me
H
Cl OCH2 COOY4 SO2 Me
H
Cl OCHMeCOOMe SO2 Me
H
Cl OCHMeCOOEt SO2 Me
H
Cl OCHMeCOOPr-i SO2 Me
H
Cl OCH2 CH2 CN
SO2 Me
H
Cl OCH2 SMe SO2 Me
H
Cl OCH2 CH2 SMe
SO2 Me
H
Cl OCH2 CH2 S(O)Me
SO2 Me
H
Cl OCH2 CH2 SO2 Me
SO2 Me
H
Cl OCH2 CH2 SPr-i
SO2 Me
H
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
H
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
H
Cl OCOOMe SO2 Me
H
Cl OCOOPr-i SO2 Me
H
Cl OCONH2 SO2 Me
H
Cl OCONHMe SO2 Me
H
Cl OCONMe2 SO2 Me
H
Cl OP(O)(OMe)2 SO2 Me
H
Cl Y20 SO2 Me
H
Cl SCH2 CHCH2
SO2 Me
H
Cl SCH2 CHCMe2
SO2 Me
H
Cl SCH2 C CH SO2 Me
H
Cl SCH2 CF3 SO2 Me
H
Cl SCH2 CCl3
SO2 Me
H
Cl Y21 SO2 Me
H
Cl SPh SO2 Me
H
Cl SCH2 CH2 OMe
SO2 Me
H
Cl SCH2 CH2 OEt
SO2 Me
H
Cl SCH2 CH2 OPr-i
SO2 Me
H
Cl Y22 SO2 Me
H
Cl S(O)CH2 CHCH2
SO2 Me
H
Cl S(O)CH2 CHCMe2
SO2 Me
H
Cl S(O)CH2 CCH SO2 Me
H
Cl S(O)CH2 CH2 Cl
SO2 Me
H
Cl Y23 SO2 Me
H
Cl SO2 CH2 CHCH2
SO2 Me
H
Cl SO2 CH2 CHCMe2
SO2 Me
H
Cl SO2 CH2 CCH
SO2 Me
H
Cl SO2 CH2 CF3
SO2 Me
H
Cl SO2 CH2 CH2 Cl
SO2 Me
H
Cl Y24 SO2 Me
H
Cl Y25 SO2 Me
H
Cl SO2 Ph SO2 Me
H
Cl SO2 CH2 CH2 OMe
SO2 Me
H
Cl SO2 CH2 CH2 OEt
SO2 Me
H
Cl SO2 CH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 OEt
SO2 Me
CH2 Ph
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCHMeCH2 OMe SO2 Me
CH2 Ph
Cl OCH2 CH2 SMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Cl SCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SCH2 CH2 OPr-i
SO2 Me
CH 2 Ph
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Cl SCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 OMe
Cl H
Cl OCH2 CH2 OEt
Cl H
Cl OCH2 CH2 OPr-i
Cl H
Cl OCHMeCH2 OMe Cl H
Cl OCH2 COOMe Cl H
Cl OCH2 CH2 SMe
Cl H
Cl OCH2 CH2 SO2 Me
Cl H
Cl SCH2 CH2 OMe
Cl H
Cl SO2 CH2 CH2 OMe
Cl H
Cl OCH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 SMe
Cl CH2 Ph
Cl OCH2 CH2 SOMe
Cl CH2 Ph
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 Ph
Cl SO2 CH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 OMe
Cl CH2 COPh
Cl OCH2 CH2 SMe
Cl CH2 COPh
Cl OCH2 CH2 SO2 Me
Cl CH2 COPh
Cl SCH2 CH2 OMe
Cl CH2 COPh
Cl SCH2 CH2 OEt
Cl CH2 COPh
Cl SO2 CH2 CH2 OMe
Cl CH2 COPh
OMe Y1 SO2 Me
H
OMe Y2 SO2 Me
H
OMe Y3 SO2 Me
H
OMe Y4 SO2 Me
H
OMe Y5 SO2 Me
H
OMe Y6 SO2 Me
H
OMe Y7 SO2 Me
H
OMe OCH2 CHCH2
SO2 Me
H
OMe OCHMeCHCH2 SO2 Me
H
OMe OCMe2 CHCH2
SO2 Me
H
OMe OCH2 CMeCH2
SO2 Me
H
OMe OCH2 CHCHMe SO2 Me
H
OMe OCH2 CHCMe2
SO2 Me
H
OMe OCH2 CH2 CHCH2
SO2 Me
H
OMe OCH2 CCH SO2 Me
H
OMe OCHMeCCH SO2 Me
H
OMe OCMe2 CCH SO2 Me
H
OMe OCH2 CCMe SO2 Me
H
OMe OCH2 CH2 F
SO2 Me
H
OMe OCH2 CHF2
SO2 Me
H
OMe OCH2 CF3 SO2 Me
H
OMe OCH2 CH2 Cl
SO2 Me
H
OMe OCH2 CCl3
SO2 Me
H
OMe OCHMeCH 2 Cl SO2 Me
H
OMe OCH2 CH2 CH2 Cl
SO2 Me
H
OMe OCH2 CH2 Br
SO2 Me
H
OMe Y8 SO2 Me
H
OMe OCH2 CClCH2
SO2 Me
H
OMe OCH2 CClCHCl SO2 Me
H
OMe OCH2 CH2 NO2
SO2 Me
H
OMe OPh SO2 Me
H
OMe OPhMe-2 SO2 Me
H
OMe OPhCl-4 SO2 Me
H
OMe OPhNO2 -4 SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OEt
SO2 Me
H
OMe OCH2 CH2 OPr-n
SO2 Me
H
OMe OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OBu-n
SO2 Me
H
OMe OCH2 CH2 OBu-i
SO2 Me
H
OMe OCH2 CH2 OBu-s
SO2 Me
H
OMe OCH2 CH2 OBu-t
SO2 Me
H
OMe OCH2 CH2Y4
SO2 Me
H
OMe OCHMeCH2 OMe SO2 Me
H
OMe OCH2 CHMeOMe SO2 Me
H
OMe OCH2 CH2 OPh
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
OMe OCH2 CH2 OH
SO2 Me
H
OMe OCH2 Ph SO2 Me
H
OMe OCHMePh SO2 Me
H
OMe OCH2 CH2 Ph
SO2 Me
H
OMe OCH2 Ph-2-Cl SO2 Me
H
OMe OCH2 Ph-3-Me SO2 Me
H
OMe OCH2 Ph-4-OMe SO2 Me
H
OMe OCH2 Ph-4-NO2
SO2 Me
H
OMe Y9 SO2 Me
H
OMe Y10 SO2 Me
H
OMe Y11 SO2 Me
H
OMe Y12 SO2 Me
H
OMe Y13 SO2 Me
H
OMe Y14 SO2 Me
H
OMe Y15 SO2 Me
H
OMe Y16 SO2 Me
H
OMe Y17 SO2 Me
H
OMe Y18 SO2 Me
H
OMe OCH2 CH2 NH2
SO2 Me
H
OMe OCH2 CH2 NHMe
SO2 Me
H
OMe OCH2 CH2 NHPr-i
SO2 Me
H
OMe OCH2 CH2 NMe2
SO2 Me
H
OMe OCH2 CH2 NEt2
SO2 Me
H
OMe Y19 SO2 Me
H
OMe OCH2 COOMe SO2 Me
H
OMe OCH2 COOEt SO2 Me
H
OMe OCH2 COOPr-i SO2 Me
H
OMe OCH2 COOBu-i SO2 Me
H
OMe OCH2 COOBu-t SO2 Me
H
OMe OCH2 COOY4 SO2 Me
H
OMe OCHMeCOOMe SO2 Me
H
OMe OCHMeCOOEt SO2 Me
H
OMe OCHMeCOOPr-i SO2 Me
H
OMe OCH2 CH2 CN
SO2 Me
H
OMe OCH2 SMe SO2 Me
H
OMe OCH2 CH2 SMe
SO2 Me
H
OMe OCH2 CH2 S(O)Me
SO2 Me
H
OMe OCH2 CH2 SO2 Me
SO2 Me
H
OMe OCH2 CH2 SPr-i
SO2 Me
H
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
H
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
H
OMe OCOOMe SO2 Me
H
OMe OCOOPr-i SO2 Me
H
OMe OCONH2 SO 2 Me
H
OMe OCONHMe SO2 Me
H
OMe OCONMe2 SO2 Me
H
OMe OP(O)(OMe)2 SO2 Me
H
OMe Y20 SO2 Me
H
OMe SCH2 CHCH2
SO2 Me
H
OMe SCH2 CHCMe2
SO2 Me
H
OMe SCH2 CCH SO2 Me
H
OMe SCH2 CF3 SO2 Me
H
OMe SCH2 CCl3
SO2 Me
H
OMe Y21 SO2 Me
H
OMe SPh SO2 Me
H
OMe SCH2 CH2 OMe
SO2 Me
H
OMe SCH2 CH2 OEt
SO2 Me
H
OMe SCH2 CH2 OPr-i
SO2 Me
H
OMe Y22 SO2 Me
H
OMe S(O)CH2 CHCH2
SO2 Me
H
OMe S(O)CH2 CHCMe2
SO2 Me
H
OMe S(O)CH2 CCH SO2 Me
H
OMe S(O)CH2 CH2 Cl
SO2 Me
H
OMe Y23 SO2 Me
H
OMe SO2 CH2 CHCH2
SO2 Me
H
OMe SO 2 CH2 CHCMe2
SO2 Me
H
OMe SO2 CH2 CCH
SO2 Me
H
OMe SO2 CH2 CF3
SO2 Me
H
OMe SO2 CH2 CH2 Cl
SO2 Me
H
OMe Y24 SO2 Me
H
OMe Y25 SO2 Me
H
OMe SO2 Ph SO2 Me
H
OMe SO2 CH2 CH2 OMe
SO2 Me
H
OMe SO2 CH2 CH2 OEt
SO2 Me
H
OMe SO2 CH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 OEt
SO2 Me
CH2 Ph
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCHMeCH2 OMe SO2 Me
CH2 Ph
OMe OCH2 CH2 SMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SPr-i
SO 2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
OMe SCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SOMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
OMe SCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe SO2 CH2 CH 2 OMe
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 OMe
Cl H
OMe OCH2 CH2 OEt
Cl H
OMe OCH2 CH2 OPr-i
Cl H
OMe OCHMeCH2 OMe Cl H
OMe OCH2 COOMe Cl H
OMe OCH2 CH2 SMe
Cl H
OMe OCH2 CH2 SO2 Me
Cl H
OMe SCH2 CH2 OMe
Cl H
OMe SO2 CH2 CH2 OMe
Cl H
OMe OCH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 SMe
Cl CH2 Ph
OMe OCH2 CH2 SOMe
Cl CH2 Ph
OMe OCH2 CH2 SO2 Me
Cl CH2 Ph
OMe SCH2 CH2 OMe
Cl CH2 Ph
OMe SO2 CH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 OMe
Cl CH2 COPh
OMe OCH2 CH2 SMe
Cl CH2 COPh
OMe OCH2 CH2 SO2 Me
Cl CH2 COPh
OMe SCH2 CH2 OMe
Cl CH2 COPh
OMe SCH2 CH2 OEt
Cl CH2 COPh
OMe SO2 CH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
Y1 SO2 Me
H
CH2 OMe
Y2 SO2 Me
H
CH2 OMe
Y3 SO2 Me
H
CH2 OMe
Y4 SO2 Me
H
CH2 OMe
Y5 SO2 Me
H
CH2 OMe
Y6 SO2 Me
H
CH2 OMe
Y7 SO2 Me
H
CH2 OMe
OCH2 CHCH2
SO2 Me
H
CH2 OMe
OCHMeCHCH2 SO2 Me
H
CH2 OMe
OCMe2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CMeCH2
SO2 Me
H
CH2 OMe
OCH2 CHCHMe SO2 Me
H
CH2 OMe
OCH2 CHCMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CCH SO2 Me
H
CH2 OMe
OCHMeCCH SO2 Me
H
CH 2 OMe
OCMe2 CCH SO2 Me
H
CH2 OMe
OCH2 CCMe SO2 Me
H
CH2 OMe
OCH2 CH2 F
SO2 Me
H
CH2 OMe
OCH2 CHF2
SO2 Me
H
CH2 OMe
OCH2 CF3 SO2 Me
H
CH2 OMe
OCH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CCl3
SO2 Me
H
CH2 OMe
OCHMeCH2 Cl SO2 Me
H
CH2 OMe
OCH2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CH2 Br
SO2 Me
H
CH2 OMe
Y8 SO2 Me
H
CH2 OMe
OCH2 CClCH2
SO2 Me
H
CH2 OMe
OCH2 CClCHCl SO2 Me
H
CH2 OMe
OCH2 CH2 NO2
SO2 Me
H
CH2 OMe
OPh SO2 Me
H
CH2 OMe
OPhMe-2 SO2 Me
H
CH2 OMe
OPhCl-4 SO2 Me
H
CH2 OMe
OPhNO2 -4 SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OEt
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-s
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-t
SO2 Me
H
CH2 OMe
OCH2 CH2Y4
SO2 Me
H
CH2 OMe
OCHMeCH2 OMe SO2 Me
H
CH2 OMe
OCH2 CHMeOMe SO2 Me
H
CH2 OMe
OCH2 CH2 OPh
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OH
SO2 Me
H
CH2 OMe
OCH2 Ph SO2 Me
H
CH2 OMe
OCHMePh SO2 Me
H
CH2 OMe
OCH2 CH2 Ph
SO2 Me
H
CH2 OMe
OCH2 Ph-2-Cl SO2 Me
H
CH2 OMe
OCH2 Ph-3-Me SO2 Me
H
CH2 OMe
OCH2 Ph-4-OMe SO2 Me
H
CH2 OMe
OCH2 Ph-4-NO2
SO2 Me
H
CH2 OMe
Y9 SO2 Me
H
CH2 OMe
Y10 SO2 Me
H
CH2 OMe
Y11 SO2 Me
H
CH2 OMe
Y12 SO2 Me
H
CH2 OMe
Y13 SO2 Me
H
CH2 OMe
Y14 SO2 Me
H
CH2 OMe
Y15 SO2 Me
H
CH2 OMe
Y16 SO2 Me
H
CH2 OMe
Y17 SO2 Me
H
CH2 OMe
Y18 SO2 Me
H
CH2 OMe
OCH2 CH2 NH2
SO2 Me
H
CH2 OMe
OCH2 CH2 NHMe
SO2 Me
H
CH2 OMe
OCH2 CH2 NHPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 NMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 NEt2
SO2 Me
H
CH2 OMe
Y19 SO2 Me
H
CH2 OMe
OCH2 COOMe SO2 Me
H
CH2 OMe
OCH2 COOEt SO2 Me
H
CH2 OMe
OCH2 COOPr-i SO2 Me
H
CH2 OMe
OCH2 COOBu-i SO2 Me
H
CH2 OMe
OCH2 COOBu-t SO2 Me
H
CH2 OMe
OCH2 COOY4 SO2 Me
H
CH2 OMe
OCHMeCOOMe SO2 Me
H
CH2 OMe
OCHMeCOOEt SO2 Me
H
CH2 OMe
OCHMeCOOPr-i SO2 Me
H
CH2 OMe
OCH2 CH2 CN
SO2 Me
H
CH2 OMe
OCH2 SMe SO2 Me
H
CH2 OMe
OCH2 CH2 SMe
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
H
CH2 OMe
OCOOMe SO2 Me
H
CH2 OMe
OCOOPr-i SO2 Me
H
CH2 OMe
OCONH2 SO2 Me
H
CH2 OMe
OCONHMe SO2 Me
H
CH2 OMe
OCONMe2 SO2 Me
H
CH2 OMe
OP(O)(OMe)2 SO2 Me
H
CH2 OMe
Y20 SO2 Me
H
CH2 OMe
SCH2 CHCH2
SO2 Me
H
CH2 OMe
SCH2 CHCMe2
SO2 Me
H
CH2 OMe
SCH2 CCH SO2 Me
H
CH2 OMe
SCH2 CF3 SO2 Me
H
CH2 OMe
SCH2 CCl3
SO2 Me
H
CH2 OMe
Y21 SO2 Me
H
CH2 OMe
SPh SO2 Me
H
CH2 OMe
SCH2 CH2 OMe
SO2 Me
H
CH2 OMe
SCH2 CH2 OEt
SO2 Me
H
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
Y22 SO2 Me
H
CH 2 OMe
S(O)CH2 CHCH2
SO2 Me
H
CH2 OMe
S(O)CH2 CHCMe2
SO2 Me
H
CH2 OMe
S(O)CH2 CCH SO2 Me
H
CH2 OMe
S(O)CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y23 SO2 Me
H
CH2 OMe
SO2 CH2 CHCH2
SO2 Me
H
CH2 OMe
SO2 CH2 CHCMe2
SO2 Me
H
CH2 OMe
SO2 CH2 CCH
SO2 Me
H
CH2 OMe
SO2 CH2 CF3
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y24 SO2 Me
H
CH2 OMe
SO2 Ph SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OEt
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OEt
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCHMeCH2 OMe SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH 2 Ph
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SOMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OEt
Cl H
CH2 OMe
OCH2 CH2 OPr-i
Cl H
CH2 OMe
OCHMeCH2 OMe Cl H
CH2 OMe
OCH2 COOMe Cl H
CH2 OMe
OCH2 CH2 SMe
Cl H
CH2 OMe
OCH2 CH2 SO2 Me
Cl H
CH2 OMe
SCH2 CH2 OMe
Cl H
CH2 OMe
SO2 CH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SOMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 Ph
CH2 OMe
SCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OEt
Cl CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 COPh
______________________________________
TABLE 7
______________________________________
##STR38##
X Y Z Q
______________________________________
Me Y1 SO2 Me
H
Me Y2 SO2 Me
H
Me Y3 SO2 Me
H
Me Y4 SO2 Me
H
Me Y5 SO2 Me
H
Me Y6 SO2 Me
H
Me Y7 SO2 Me
H
Me OCH2 CHCH2
SO2 Me
H
Me OCHMeCHCH2 SO2 Me
H
Me OCMe2 CHCH2
SO2 Me
H
Me OCH2 CMeCH2
SO2 Me
H
Me OCH2 CHCHMe SO2 Me
H
Me OCH2 CHCMe2
SO2 Me
H
Me OCH2 CH2 CHCH2
SO2 Me
H
Me OCH2 CCH SO2 Me
H
Me OCHMeC CH SO2 Me
H
Me OCMe2 CCH SO2 Me
H
Me OCH2 CCMe SO2 Me
H
Me OCH2 CH2 F
SO2 Me
H
Me OCH2 CHF2
SO2 Me
H
Me OCH2 CF3 SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CCl3
SO2 Me
H
Me OCHMeCH2 Cl SO2 Me
H
Me OCH2 CH2 CH2 Cl
SO2 Me
H
Me OCH2 CH2 Br
SO2 Me
H
Me Y8 SO2 Me
H
Me OCH2 CClCH2
SO2 Me
H
Me OCH2 CClCHCl SO2 Me
H
Me OCH2 CH2 NO2
SO2 Me
H
Me OPh SO2 Me
H
Me OPhMe-2 SO2 Me
H
Me OPhCl-4 SO2 Me
H
Me OPhNO2 -4 SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OEt
SO 2 Me
H
Me OCH2 CH2 OPr-n
SO2 Me
H
Me OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OBu-n
SO2 Me
H
Me OCH2 CH2 OBu-i
SO2 Me
H
Me OCH2 CH2 OBu-s
SO2 Me
H
Me OCH2 CH2 OBu-t
SO2 Me
H
Me OCH2 CH2 -Y4
SO2 Me
H
Me OCHMeCH2 OMe SO2 Me
H
Me OCH2 CHMeOMe SO2 Me
H
Me OCH2 CH2 OPh
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Me OCH2 CH2 OH
SO2 Me
H
Me OCH2 Ph SO2 Me
H
Me OCHMePh SO2 Me
H
Me OCH2 CH2 Ph
SO2 Me
H
Me OCH2 Ph-2-Cl SO2 Me
H
Me OCH2 Ph-3-Me SO2 Me
H
Me OCH2 Ph-4-OMe SO2 Me
H
Me OCH2 Ph-4-NO2
SO2 Me
H
Me Y9 SO2 Me
H
Me Y10 SO2 Me
H
Me Y11 SO2 Me
H
Me Y12 SO2 Me
H
Me Y13 SO2 Me
H
Me Y14 SO2 Me
H
Me Y15 SO2 Me
H
Me Y16 SO2 Me
H
Me Y17 SO2 Me
H
Me Y18 SO2 Me
H
Me OCH2 CH2 NH2
SO2 Me
H
Me OCH2 CH2 NHMe
SO2 Me
H
Me OCH2 CH2 NHPr-i
SO2 Me
H
Me OCH2 CH2 NMe2
SO2 Me
H
Me OCH2 CH2 NEt2
SO2 Me
H
Me Y19 SO2 Me
H
Me OCH2 COOMe SO2 Me
H
Me OCH2 COOEt SO2 Me
H
Me OCH2 COOPr-i SO2 Me
H
Me OCH2 COOBu-i SO2 Me
H
Me OCH2 COOBu-t SO2 Me
H
Me OCH2 COO-Y4 SO2 Me
H
Me OCHMeCOOMe SO2 Me
H
Me OCHMeCOOEt SO2 Me
H
Me OCHMeCOOPr-i SO2 Me
H
Me OCH2 CH2 CN
SO2 Me
H
Me OCH2 SMe SO2 Me
H
Me OCH2 CH2 SMe
SO2 Me
H
Me OCH2 CH2 S(O)Me
SO2 Me
H
Me OCH2 CH2 SO2 Me
SO2 Me
H
Me OCH2 CH2 SPr-i
SO2 Me
H
Me OCH2 CH2 S(O)Pr-i
SO2 Me
H
Me OCH2 CH2 SO2 Pr-i
SO2 Me
H
Me OCOOMe SO2 Me
H
Me OCOOPr-i SO2 Me
H
Me OCONHG2 SO2 Me
H
Me OCONHMe SO2 Me
H
Me OCONMe2 SO2 Me
H
Me OP(O)(OMe)2 SO2 Me
H
Me Y20 SO2 Me
H
Me SCH2 CHCH2
SO2 Me
H
Me SCH2 CHCMe2
SO2 Me
H
Me SCH2 CCH SO2 Me
H
Me SCH2 CF3 SO2 Me
H
Me SCH2 CCl3
SO2 Me
H
Me Y21 SO2 Me
H
Me SPh SO2 Me
H
Me SCH2 CH2 OMe
SO2 Me
H
Me SCH2 CH 2 OEt
SO2 Me
H
Me SCH2 CH2 OPr-i
SO2 Me
H
Me Y22 SO2 Me
H
Me S(O)CH2 CHCH2
SO2 Me
H
Me S(O)CH2 CHCMe2
SO2 Me
H
Me S(O)CH2 CCH SO2 Me
H
Me S(O)CH2 CH2 Cl
SO2 Me
H
Me Y23 SO2 Me
H
Me SO2 CH2 CHCH2
SO2 Me
H
Me SO2 CH2 CHCMe2
SO2 Me
H
Me SO2 CH2 CCH
SO2 Me
H
Me SO2 CH2 CF3
SO2 Me
H
Me SO2 CH2 CH2 Cl
SO2 Me
H
Me Y24 SO2 Me
H
Me Y25 SO2 Me
H
Me SO2 Ph SO2 Me
H
Me SO2 CH2 CH2 OMe
SO2 Me
H
Me SO2 CH2 CH2 OEt
SO2 Me
H
Me SO2 CH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
CH2 Ph
Me OCH2 CH2 OEt
SO2 Me
CH2 Ph
Me OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCHMeCH2 OMe SO2 Me
CH2 Ph
Me OCH2 CH2 SMe
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Me SCH2 CH2 OMe
SO2 Me
CH2 Ph
Me SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 OMe
SO2 Me
CH2 COPh
Me OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Me OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Me SCH2 CH2 OMe
SO2 Me
CH2 COPh
Me SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 OMe
Cl H
Me OCH2 CH2 OEt
Cl H
Me OCH2 CH2 OPr-i
Cl H
Me OCHMeCH2 OMe Cl H
Me OCH2 COOMe Cl H
Me OCH2 CH2 SMe
Cl H
Me OCH2 CH2 SO2 Me
Cl H
Me SCH2 CH2 OMe
Cl H
Me SO2 CH2 CH2 OMe
Cl H
Me OCH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 SMe
Cl CH2 Ph
Me OCH2 CH2 SOMe
Cl CH2 Ph
Me OCH2 CH2 SO2 Me
Cl CH2 Ph
Me SCH2 CH2 OMe
Cl CH2 Ph
Me SO2 CH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 OMe
Cl CH2 COPh
Me OCH2 CH2 SMe
Cl CH2 COPh
Me OCH2 CH2 SO2 Me
Cl CH2 COPh
Me SCH2 CH2 OMe
Cl CH2 COPh
Me SCH2 CH2 OEt
Cl CH2 COPh
Me SO2 CH2 CH2 OMe
Cl CH2 COPh
Cl Y1 SO2 Me
H
Cl Y2 SO2 Me
H
Cl Y3 SO2 Me
H
Cl Y4 SO2 Me
H
Cl Y5 SO2 Me
H
Cl Y6 SO2 Me
H
Cl Y7 SO2 Me
H
Cl OCH2 CHCH2
SO2 Me
H
Cl OCHMeCHCH2 SO2 Me
H
Cl OCMe2 CHCH2
SO2 Me
H
Cl OCH2 CMeCH2
SO2 Me
H
Cl OCH2 CHCHMe SO2 Me
H
Cl OCH2 CHCMe2
SO2 Me
H
Cl OCH2 CH2 CHCH2
SO2 Me
H
Cl OCH2 CCH SO2 Me
H
Cl OCHMeCCH SO2 Me
H
Cl OCMe2 CCH SO2 Me
H
Cl OCH2 CCMe SO2 Me
H
Cl OCH2 CH2 F
SO2 Me
H
Cl OCH2 CHF2
SO2 Me
H
Cl OCH2 CF3 SO2 Me
H
Cl OCH2 CH2 Cl
SO2 Me
H
Cl OCH2 CCl3
SO2 Me
H
Cl OCHMeCH2 Cl SO2 Me
H
Cl OCH2 CH2 CH2 Cl
SO2 Me
H
Cl OCH2 CH2 Br
SO2 Me
H
Cl Y8 SO2 Me
H
Cl OCH2 CClCH2
SO2 Me
H
Cl OCH2 CClCHCl SO2 Me
H
Cl OCH2 CH2 NO 2
SO2 Me
H
Cl OPh SO2 Me
H
Cl OPh-Me-2 SO2 Me
H
Cl OPh-Cl-4 SO2 Me
H
Cl OPh-NO2 -4 SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OEt
SO2 Me
H
Cl OCH2 CH2 OPr-n
SO2 Me
H
Cl OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OBu-n
SO2 Me
H
Cl OCH2 CH2 OBu-i
SO2 Me
H
Cl OCH2 CH2 OBu-s
SO2 Me
H
Cl OCH2 CH2 OBu-t
SO2 Me
H
Cl OCH2 CH2-Y4
SO2 Me
H
Cl OCHMeCH2 OMe SO2 Me
H
Cl OCH2 CHMeOMe SO2 Me
H
Cl OCH2 CH2 OPh
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Cl OCH2 CH2 OH
SO2 Me
H
Cl OCH2 Ph SO2 Me
H
Cl OCHMePh SO2 Me
H
Cl OCH2 CH2 Ph
SO2 Me
H
Cl OCH2 Ph-2-Cl SO2 Me
H
Cl OCH2 Ph-3-Me SO2 Me
H
Cl OCH2 Ph-4-OMe SO2 Me
H
Cl OCH2 Ph-4-NO2
SO2 Me
H
Cl Y9 SO2 Me
H
Cl Y10 SO2 Me
H
Cl Y11 SO2 Me
H
Cl Y12 SO2 Me
H
Cl Y13 SO2 Me
H
Cl Y14 SO2 Me
H
Cl Y15 SO2 Me
H
Cl Y16 SO2 Me
H
Cl Y17 SO2 Me
H
Cl Y18 SO2 Me
H
Cl OCH2 CH2 NH2
SO2 Me
H
Cl OCH2 CH2 NHMe
SO2 Me
H
Cl OCH2 CH2 NHPr-i
SO2 Me
H
Cl OCH2 CH2 NMe2
SO2 Me
H
Cl OCH2 CH2 NEt2
SO2 Me
H
Cl Y19 SO2 Me
H
Cl OCH2 COOMe SO2 Me
H
Cl OCH2 COOEt SO2 Me
H
Cl OCH2 COOPr-i SO2 Me
H
Cl OCH2 COOBu-i SO2 Me
H
Cl OCH2 COOBu-t SO2 Me
H
Cl OCH2 COO-Y4 SO2 Me
H
Cl OCHMeCOOMe SO2 Me
H
Cl OCHMeCOOEt SO2 Me
H
Cl OCHMeCOOPr-i SO2 Me
H
Cl OCH2 CH2 CN
SO2 Me
H
Cl OCH2 SMe SO2 Me
H
Cl OCH2 CH2 SMe
SO2 Me
H
Cl OCH2 CH2 S(O)Me
SO2 Me
H
Cl OCH2 CH2 SO2 Me
SO2 Me
H
Cl OCH2 CH2 SPr-i
SO2 Me
H
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
H
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
H
Cl OCOOMe SO2 Me
H
Cl OCOOPr-i SO2 Me
H
Cl OCONH2 SO2 Me
H
Cl OCONHMe SO2 Me
H
Cl OCONMe2 SO2 Me
H
Cl OP(O)(OMe)2 SO2 Me
H
Cl Y20 SO2 Me
H
Cl SCH2 CHCH2
SO2 Me
H
Cl SCH2 CHCMe2
SO2 Me
H
Cl SCH2 CCH SO 2 Me
H
Cl SCH2 CF3 SO2 Me
H
Cl SCH2 CCl3
SO2 Me
H
Cl Y21 SO2 Me
H
Cl SPh SO2 Me
H
Cl SCH2 CH2 OMe
SO2 Me
H
Cl SCH2 CH2 OEt
SO2 Me
H
Cl SCH2 CH2 OPr-i
SO2 Me
H
Cl Y22 SO2 Me
H
Cl S(O)CH2 CHCH2
SO2 Me
H
Cl S(O)CH2 CHCMe2
SO2 Me
H
Cl S(O)CH2 CCH SO2 Me
H
Cl S(O)CH2 CH2 Cl
SO2 Me
H
Cl Y23 SO2 Me
H
Cl SO2 CH2 CHCH2
SO2 Me
H
Cl SO2 CH2 CHCMe2
SO2 Me
H
Cl SO2 CH2 CCH
SO2 Me
H
Cl SO2 CH2 CF3
SO2 Me
H
Cl SO2 CH2 CH2 Cl
SO2 Me
H
Cl Y24 SO2 Me
H
Cl Y25 SO2 Me
H
Cl SO2 Ph SO2 Me
H
Cl SO2 CH2 CH2 OMe
SO2 Me
H
Cl SO2 CH2 cH2 OEt
SO2 Me
H
Cl SO2 CH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 OEt
SO2 Me
CH2 Ph
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCHMeCH2 OMe SO2 Me
CH2 Ph
Cl OCH2 CH2 SMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Cl OCH3 CH2 SO2 Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Cl SCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Cl SCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 OMe
Cl H
Cl OCH2 CH2 OEt
Cl H
Cl OCH2 CH2 OPr-i
Cl H
Cl OCHMeCH2 OMe Cl H
Cl OCH2 COOMe Cl H
Cl OCH2 CH 2 SMe
Cl H
Cl OCH2 CH2 SO2 Me
Cl H
Cl SCH2 CH2 OMe
Cl H
Cl SO2 CH2 CH2 OMe
Cl H
Cl OCH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 SMe
Cl CH2 Ph
Cl OCH2 CH2 SOMe
Cl CH2 Ph
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 Ph
Cl SO2 CH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 OMe
Cl CH2 COPh
Cl OCH2 CH2 SMe
Cl CH2 COPh
Cl OCH2 CH2 SO2 Me
Cl CH2 COPh
Cl SCH2 CH2 OMe
Cl CH2 COPh
Cl SCH2 CH2 OEt
Cl CH2 COPh
Cl SO2 CH2 CH2 OMe
Cl CH2 COPh
OMe Y1 SO2 Me
H
OMe Y2 SO2 Me
H
OMe Y3 SO2 Me
H
OMe Y4 SO2 Me
H
OMe Y5 SO2 Me
H
OMe Y6 SO2 Me
H
OMe Y7 SO2 Me
H
OMe OCH2 CHCH2
SO2 Me
H
OMe OCHMdCHCH2 SO2 Me
H
OMe OCMe2 CHCH2
SO2 Me
H
OMe OCH2 CMeCH2
SO2 Me
H
OMe OCH2 CHCHMe SO2 Me
H
OMe OCH2 CHCMe2
SO2 Me
H
OMe OCH2 CH2 CHCH2
SO2 Me
H
OMe OCH2 CCH SO2 Me
H
OMe OCHMeCCH SO2 Me
H
OMe OCMe2 CCH SO2 Me
H
OMe OCH2 CCMe SO2 Me
H
OMe OCH2 CH2 F
SO2 Me
H
OMe OCH2 CHF2
SO2 Me
H
OMe OCH2 CF3 SO2 Me
H
OMe OCH2 CH2 Cl
SO2 Me
H
OMe OCH2 CCl3
SO2 Me
H
OMe OCHMeCH2 Cl SO2 Me
H
OMe OCH2 CH 2 CH2 Cl
SO2 Me
H
OMe OCH2 CH2 Br
SO2 Me
H
OMe Y8 SO2 Me
H
OMe OCH2 CClCH2
SO2 Me
H
OMe OCH2 CClCHCl SO2 Me
H
OMe OCH2 CH2 NO2
SO2 Me
H
OMe OPh SO2 Me
H
OMe OPhMe-2 SO2 Me
H
OMe OPhCl-4 SO2 Me
H
OMe OPhNO2 -4 SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OEt
SO2 Me
H
OMe OCH2 CH2 OPr-n
SO2 Me
H
OMe OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OBu-n
SO2 Me
H
OMe OCH2 CH2 OBu-i
SO2 Me
H
OMe OCH2 CH2 OBu-s
SO2 Me
H
OMe OCH2 CH2 OBu-t
SO2 Me
H
OMe OCH2 CH2 -Y4
SO2 Me
H
OMe OCHMeCH2 OMe SO2 Me
H
OMe OCH2 CHMeOMe SO2 Me
H
OMe OCH2 CH2 OPh
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
OMe OCH2 CH2 OH
SO2 Me
H
OMe OCH2 Ph SO2 Me
H
OMe OCHMePh SO2 Me
H
OMe OCH2 CH2 Ph
SO2 Me
H
OMe OCH2 Ph-2-Cl SO2 Me
H
OMe OCH2 Ph-3-Me SO2 Me
H
OMe OCH2 Ph-4-OMe SO2 Me
H
OMe OCH2 Ph-4-NO2
SO2 Me
H
OMe Y9 SO2 Me
H
OMe Y10 SO2 Me
H
OMe Y11 SO2 Me
H
OMe Y12 SO2 Me
H
OMe Y13 SO2 Me
H
OMe Y14 SO2 Me
H
OMe Y15 SO2 Me
H
OMe Y16 SO2 Me
H
OMe Y17 SO2 Me
H
OMe Y18 SO2 Me
H
OMe OCH2 CH2 NH2
SO2 Me
H
OMe OCH2 CH2 NHMe
SO2 Me
H
OMe OCH2 CH2 NHPr-i
SO2 Me
H
OMe OCH2 CH2 NMe2
SO2 Me
H
OMe OCH2 CH2 NEt2
SO2 Me
H
OMe Y19 SO2 Me
H
OMe OCH2 COOMe SO2 Me
H
OMe OCH2 COOEt SO2 Me
H
OMe OCH2 COOPr-i SO2 Me
H
OMe OCH2 COOBu-i SO2 Me
H
OMe OCH2 COOBu-t SO2 Me
H
OMe OCH2 COO-Y4 SO2 Me
H
OMe OCHMeCOOMe SO2 Me
H
OMe OCHMeCOOEt SO2 Me
H
OMe OCHMeCOOPr-i SO2 Me
H
OMe OCH2 CH2 CN
SO2 Me
H
OMe OCH2 SMe SO2 Me
H
OMe OCH2 CH2 SMe
SO2 Me
H
OMe OCH2 CH2 S(O)Me
SO2 Me
H
OMe OCH2 CH2 SO2 Me
SO2 Me
H
OMe OCH2 CH2 SPr-i
SO2 Me
H
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
H
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
H
OMe OCOOMe SO2 Me
H
OMe OCOOPr-i SO2 Me
H
OMe OCONH2 SO2 Me
H
OMe OCONHMe SO2 Me
H
OMe OCONMe 2 SO2 Me
H
OMe OP(O)(OMe)2 SO2 Me
H
OMe Y20 SO2 Me
H
OMe SCH2 CHCH2
SO2 Me
H
OMe SCH2 CHCMe2
SO2 Me
H
OMe SCH2 CCH SO2 Me
H
OMe SCH2 CF3 SO2 Me
H
OMe SCH2 CCl3
SO2 Me
H
OMe Y21 SO2 Me
H
OMe SPh SO2 Me
H
OMe SCH2 CH2 OMe
SO2 Me
H
OMe SCH2 CH2 OEt
SO2 Me
H
OMe SCH2 CH2 OPr-i
SO2 Me
H
OMe Y22 SO2 Me
H
OMe S(O)CH2 CHCH2
SO2 Me
H
OMe S(O)CH2 CHCMe2
SO2 Me
H
OMe S(O)CH2 CCH SO2 Me
H
OMe S(O)CH2 CH2 Cl
SO2 Me
H
OMe Y23 SO2 Me
H
OMe SO2 CH2 CHCH2
SO2 Me
H
OMe SO2 CH2 CHCMe2
SO2 Me
H
OMe SO2 CH2 CCH
SO2 Me
H
OMe SO2 CH2 CF3
SO2 Me
H
OMe SO2 CH2 CH2 Cl
SO2 Me
H
OMe Y24 SO2 Me
H
OMe Y25 SO2 Me
H
OMe SO2 Ph SO2 Me
H
OMe SO2 CH2 CH2 OMe
SO2 Me
H
OMe SO2 CH2 CH2 OEt
SO2 Me
H
OMe SO2 CH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 OEt
SO2 Me
CH2 Ph
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCHMeCH2 OMe SO2 Me
CH2 Ph
OMe OCH2 CH2 SMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
OMe OCH 2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
OMe SCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SOMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Me
SO1 Me
CH2 COPh
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
OMe SCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OMe
SO2 Me
CH 2 COPh
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 OMe
Cl H
OMe OCH2 CH2 OEt
Cl H
OMe OCH2 CH2 OPr-i
Cl H
OMe OCHMeCH2 OMe Cl H
OMe OCH2 COOMe Cl H
OMe OCH2 CH2 SMe
Cl H
OMe OCH2 CH2 SO2 Me
Cl H
OMe SCH2 CH2 OMe
Cl H
OMe SO2 CH2 CH2 OMe
Cl H
OMe OCH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 SMe
Cl CH2 Ph
OMe OCH2 CH2 SOMe
Cl CH2 Ph
OMe OCH2 CH2 SO2 Me
Cl CH2 Ph
OMe SCH2 CH2 OMe
Cl CH2 Ph
OMe SO2 CH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 OMe
Cl CH2 COPh
OMe OCH2 CH2 SMe
Cl CH2 COPh
OMe OCH2 CH2 SO2 Me
Cl CH2 COPh
OMe SCH2 CH2 OMe
Cl CH2 COPh
OMe SCH2 CH2 OEt
Cl CH2 COPh
OMe SO2 CH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
Y1 SO2 Me
H
CH2 OMe
Y2 SO2 Me
H
CH2 OMe
Y3 SO2 Me
H
CH2 OMe
Y4 SO2 Me
H
CH2 OMe
Y5 SO2 Me
H
CH2 OMe
Y6 SO2 Me
H
CH2 OMe
Y7 SO2 Me
H
CH2 OMe
OCH2 CHCH2
SO2 Me
H
CH2 OMe
OCHMeCHCH2 SO2 Me
H
CH2 OMe
OCMe2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CMeCH2
SO2 Me
H
CH2 OMe
OCH2 CHCHMe SO2 Me
H
CH2 OMe
OCH2 CHCMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CCH SO2 Me
H
CH2 OMe
OCHMeCCH SO2 Me
H
CH2 OMe
OCMe2 C CH SO2 Me
H
CH2 OMe
OCH2 CCMe SO2 Me
H
CH2 OMe
OCH2 CH2 F
SO2 Me
H
CH2 OMe
OCH2 CHF2
SO2 Me
H
CH2 OMe
OCH2 CF3 SO2 Me
H
CH2 OMe
OCH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CCl3
SO2 Me
H
CH2 OMe
OCHMeCH2 Cl SO2 Me
H
CH2 OMe
OCH2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CH2 Br
SO2 Me
H
CH2 OMe
Y8 SO2 Me
H
CH2 OMe
OCH2 CClCH2
SO2 Me
H
CH2 OMe
OCH2 CClCHCl SO2 Me
H
CH2 OMe
OCH2 CH2 NO2
SO2 Me
H
CH2 OMe
OPh SO2 Me
H
CH2 OMe
OPhMe-2 SO2 Me
H
CH2 OMe
OPhCl-4 SO2 Me
H
CH2 OMe
OPh N2 -4 SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OEt
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-s
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-t
SO2 Me
H
CH2 OMe
OCH2 CH2 -Y4
SO2 Me
H
CH2 OMe
OCHMeCH2 OMe SO2 Me
H
CH2 OMe
OCH2 CHMeOMe SO2 Me
H
CH2 OMe
OCH2 CH2 OPh
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OH
SO2 Me
H
CH2 OMe
OCH2 Ph SO2 Me
H
CH2 OMe
OCHMePh SO2 Me
H
CH2 OMe
OCH2 CH2 Ph
SO2 Me
H
CH2 OMe
OCH2 Ph-2-Cl SO2 Me
H
CH2 OMe
OCH2 Ph-3-Me SO2 Me
H
CH2 OMe
OCH2 Ph-4-OMe SO2 Me
H
CH2 OMe
OCH2 Ph-4-NO2
SO2 Me
H
CH2 OMe
Y9 SO2 Me
H
CH2 OMe
Y10 SO2 Me
H
CH2 OMe
Y11 SO2 Me
H
CH2 OMe
Y12 SO2 Me
H
CH2 OMe
Y13 SO2 Me
H
CH2 OMe
Y14 SO2 Me
H
CH2 OMe
Y15 SO2 Me
H
CH2 OMe
Y16 SO2 Me
H
CH2 OMe
Y17 SO2 Me
H
CH2 OMe
Y18 SO2 Me
H
CH2 OMe
OCH2 CH2 NH2
SO2 Me
H
CH2 OMe
OCH2 CH2 NHMe
SO2 Me
H
CH2 OMe
OCH2 CH2 NHPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 NMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 NEt2
SO2 Me
H
CH2 OMe
Y19 SO2 Me
H
CH2 OMe
OCH2 COOMe SO2 Me
H
CH2 OMe
OCH2 COOEt SO2 Me
H
CH2 OMe
OCH2 COOPr-i SO2 Me
H
CH2 OMe
OCH2 COOBu-i SO2 Me
H
CH2 OMe
OCH2 COOBu-t SO2 Me
H
CH2 OMe
OCH2 COO-Y4 SO2 Me
H
CH2 OMe
OCHMeCOOMe SO2 Me
H
CH2 OMe
OCHMeCOOEt SO2 Me
H
CH2 OMe
OCHMeCOOPr-i SO2 Me
H
CH2 OMe
OCH2 CH2 CN
SO2 Me
H
CH2 OMe
OCH2 SMe SO2 Me
H
CH2 OMe
OCH2 CH2 SMe
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
H
CH2 OMe
OCOOMe SO2 Me
H
CH2 OMe
OCOOPr-i SO2 Me
H
CH2 OMe
OCONH2 SO2 Me
H
CH2 OMe
OCONHMe SO2 Me
H
CH2 OMe
OCONMe2 SO2 Me
H
CH2 OMe
OP(O)(OMe)2 SO2 Me
H
CH2 OMe
Y20 SO2 Me
H
CH2 OMe
SCH2 CHCH2
SO2 Me
H
CH2 OMe
SCH2 CHCMe2
SO2 Me
H
CH2 OMe
SCH2 CCH SO2 Me
H
CH2 OMe
SCH2 CF3 SO2 Me
H
CH2 OMe
SCH2 CCl3
SO2 Me
H
CH2 OMe
Y21 SO2 Me
H
CH2 OMe
SPh SO2 Me
H
CH2 OMe
SCH2 CH2 OMe
SO2 Me
H
CH2 OMe
SCH2 CH2 OEt
SO2 Me
H
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
Y22 SO2 Me
H
CH2 OMe
S(O)CH2 CH CH2
SO2 Me
H
CH2 OMe
S(O)CH2 CHCMe2
SO2 Me
H
CH2 OMe
S(O)CH2 CCH SO2 Me
H
CH2 OMe
S(O)CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y23 SO2 Me
H
CH2 OMe
SO2 CH2 CHCH2
SO2 Me
H
CH2 OMe
SO2 CH2 CHCMe2
SO2 Me
H
CH2 OMe
SO2 CH2 CCH
SO2 Me
H
CH2 OMe
SO2 CH2 CF3
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y24 SO2 Me
H
CH2 OMe
SO2 Ph SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OEt
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OEt
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCHMeCH2 OMe SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SOMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OEt
Cl H
CH2 OMe
OCH2 CH2 OPr-i
Cl H
CH2 OMe
OCHMeCH2 OMe Cl H
CH2 OMe
OCH2 COOMe Cl H
CH2 OMe
OCH2 CH2 SMe
Cl H
CH2 OMe
OCH2 CH2 SO2 Me
Cl H
CH2 OMe
SCH2 CH2 OMe
Cl H
CH2 OMe
SO2 CH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SOMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 Ph
CH2 OMe
SCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OEt
Cl CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 COPh
______________________________________
TABLE 8
______________________________________
##STR39##
X Y Z Q
______________________________________
Me Y1 SO2 Me
H
Me Y2 SO2 Me
H
Me Y3 SO2 Me
H
Me Y4 SO2 Me
H
Me Y5 SO2 Me
H
Me Y6 SO2 Me
H
Me Y7 SO2 Me
H
Me OCH2 CHCH2
SO2 Me
H
Me OCHMeCHCH2 SO2 Me
H
Me OCMe2 CHCH2
SO2 Me
H
Me OCH2 CMeCH2
SO2 Me
H
Me OCH2 CHCHMe SO2 Me
H
Me OCH2 CHCMe2
SO2 Me
H
Me OCH2 CH2 CHCH2
SO2 Me
H
Me OCH2 CCH SO2 Me
H
Me OCHMeC CH SO2 Me
H
Me OCMe2 CCH SO2 Me
H
Me OCH2 CCMe SO2 Me
H
Me OCH2 CH2 F
SO2 Me
H
Me OCH2 CHF2
SO2 Me
H
Me OCH2 CF3 SO2 Me
H
Me OCH2 CH2 Cl
SO2 Me
H
Me OCH2 CCl3
SO2 Me
H
Me OCHMeCH2 Cl SO2 Me
H
Me OCH2 CH2 CH2 Cl
SO2 Me
H
Me OCH2 CH2 Br
SO2 Me
H
Me Y8 SO2 Me
H
Me OCH2 CClCH2
SO2 Me
H
Me OCH2 CClCHCl SO2 Me
H
Me OCH2 CH2 NO2
SO2 Me
H
Me OPh SO2 Me
H
Me OPhMe-2 SO2 Me
H
Me OPhCl-4 SO2 Me
H
Me OPhNO2 -4 SO2 Me
H
Me OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OEt
SO2 Me
H
Me OCH2 CH2 OPr-n
SO2 Me
H
Me OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OBu-n
SO2 Me
H
Me OCH2 CH2 OBu-i
SO2 Me
H
Me OCH2 CH2 OBu-s
SO2 Me
H
Me OCH2 CH2 OBu-t
SO2 Me
H
Me OCH2 CH2 Y4
SO2 Me
H
Me OCHMeCH2 OMe SO2 Me
H
Me OCH2 CHMeOMe SO2 Me
H
Me OCH2 CH2 OPh
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Me OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Me OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Me OCH2 CH2 OH
SO2 Me
H
Me OCH2 Ph SO2 Me
H
Me OCHMePh SO2 Me
H
Me OCH2 CH2 Ph
SO2 Me
H
Me OCH2 Ph-2-Cl SO2 Me
H
Me OCH2 Ph-3-Me SO2 Me
H
Me OCH2 Ph-4-OMe SO2 Me
H
Me OCH2 Ph-4-NO2
SO2 Me
H
Me Y9 SO2 Me
H
Me Y10 SO2 Me
H
Me Y11 SO2 Me
H
Me Y12 SO2 Me
H
Me Y13 SO2 Me
H
Me Y14 SO2 Me
H
Me Y15 SO2 Me
H
Me Y16 SO2 Me
H
Me Y17 SO2 Me
H
Me Y18 SO2 Me
H
Me OCH2 CH2 NH2
SO2 Me
H
Me OCH2 CH2 NHMe
SO2 Me
H
Me OCH2 CH2 NHPr-i
SO2 Me
H
Me OCH2 CH2 NMe2
SO2 Me
H
Me OCH2 CH2 NEt2
SO2 Me
H
Me Y19 SO2 Me
H
Me OCH2 COOMe SO2 Me
H
Me OCH2 COOEt SO2 Me
H
Me OCH2 COOPr-i SO2 Me
H
Me OCH2 COOBu-i SO2 Me
H
Me OCH2 COOBu-t SO2 Me
H
Me OCH2 COOY4 SO2 Me
H
Me OCHMeCOOMe SO2 Me
H
Me OCHMeCOOEt SO2 Me
H
Me OCHMeCOOPr-i SO2 Me
H
Me OCH2 CH2 CN
SO2 Me
H
Me OCH2 SMe SO2 Me
H
Me OCH2 CH2 SMe
SO2 Me
H
Me OCH2 CH2 S(O)Me
SO2 Me
H
Me OCH2 CH2 SO2 Me
SO2 Me
H
Me OCH2 CH2 SPr-i
SO2 Me
H
Me OCH2 CH2 S(O)Pr-i
SO2 Me
H
Me OCH2 CH2 SO2 Pr-i
SO2 Me
H
Me OCOOMe SO2 Me
H
Me OCOOPr-i SO2 Me
H
Me OCONH2 SO2 Me
H
Me OCONHMe SO2 Me
H
Me OCONMe2 SO2 Me
H
Me OP(O)(OMe)2 SO2 Me
H
Me Y20 SO2 Me
H
Me SCH2 CHCH2
SO2 Me
H
Me SCH2 CHCMe2
SO2 Me
H
Me SCH2 CCH SO2 Me
H
Me SCH2 CF3 SO2 Me
H
Me SCH2 CCl3
SO2 Me
H
Me Y21 SO2 Me
H
Me SPh SO2 Me
H
Me SCH2 CH2 OMe
SO2 Me
H
Me SCH2 CH 2 OEt
SO2 Me
H
Me SCH2 CH2 OPr-i
SO2 Me
H
Me Y22 SO2 Me
H
Me S(O)CH2 CHCH2
SO2 Me
H
Me S(O)CH2 CHCMe2
SO2 Me
H
Me S(O)CH2 CCH SO2 Me
H
Me S(O)CH2 CH2 Cl
SO2 Me
H
Me Y23 SO2 Me
H
Me SO2 CH2 CHCH2
SO2 Me
H
Me SO2 CH2 CHCMe2
SO2 Me
H
Me SO2 CH2 CCH
SO2 Me
H
Me SO2 CH2 CF3
SO2 Me
H
Me SO2 CH2 CH2 Cl
SO2 Me
H
Me Y24 SO2 Me
H
Me Y25 SO2 Me
H
Me SO2 Ph SO2 Me
H
Me SO2 CH2 CH2 OMe
SO2 Me
H
Me SO2 CH2 CH2 OEt
SO2 Me
H
Me SO2 CH2 CH2 OPr-i
SO2 Me
H
Me OCH 2 CH2 OMe
SO2 Me
CH2 Ph
Me OCH2 CH2 OEt
SO2 Me
CH2 Ph
Me OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCHMeCH2 OMe SO2 Me
CH2 Ph
Me OCH2 CH2 SMe
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Me OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Me SCH2 CH2 OMe
SO2 Me
CH2 Ph
Me SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Me OCH2 CH2 OMe
SO2 Me
CH2 COPh
Me OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH 2 SMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Me OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Me SCH2 CH2 OMe
SO2 Me
CH2 COPh
Me SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Me SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Me OCH2 CH2 OMe
Cl H
Me OCH2 CH2 OEt
Cl H
Me OCH2 CH2 OPr-i
Cl H
Me OCHMeCH2 OMe Cl H
Me OCH2 COOMe Cl H
Me OCH2 CH2 SMe
Cl H
Me OCH2 CH2 SO2 Me
Cl H
Me SCH2 CH2 OMe
Cl H
Me SO2 CH2 CH2 OMe
Cl H
Me OCH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 SMe
Cl CH2 Ph
Me OCH2 CH2 SOMe
Cl CH2 Ph
Me OCH2 CH2 SO2 Me
Cl CH2 Ph
Me SCH2 CH2 OMe
Cl CH2 Ph
Me SO2 CH2 CH2 OMe
Cl CH2 Ph
Me OCH2 CH2 OMe
Cl CH2 COPh
Me OCH2 CH2 SMe
Cl CH2 COPh
Me OCH2 CH2 SO2 Me
Cl CH2 COPh
Me SCH2 CH2 OMe
Cl CH2 COPh
Me SCH2 CH2 OEt
Cl CH2 COPh
Me SO2 CH2 CH2 OMe
Cl CH2 COPh
Cl Y1 SO2 Me
H
Cl Y2 SO2 Me
H
Cl Y3 SO2 Me
H
Cl Y4 SO2 Me
H
Cl Y5 SO2 Me
H
Cl Y6 SO2 Me
H
Cl Y7 SO2 Me
H
Cl OCH2 CHCH2
SO2 Me
H
Cl OCHMeCHCH2 SO2 Me
H
Cl OCMe2 CHCH2
SO2 Me
H
Cl OCH2 CMeCH2
SO2 Me
H
Cl OCH2 CHCHMe SO2 Me
H
Cl OCH2 CHCMe2
SO2 Me
H
Cl OCH2 CH2 CHCH2
SO2 Me
H
Cl OCH2 CCH SO2 Me
H
Cl OCHMeCCH SO2 Me
H
Cl OCMe2 CCH SO2 Me
H
Cl OCH2 CCMe SO2 Me
H
Cl OCH2 CH2 F
SO2 Me
H
Cl OCH2 CHF2
SO2 Me
H
Cl OCH2 CF3 SO2 Me
H
Cl OCH2 CH2 Cl
SO2 Me
H
Cl OCH2 CCl3
SO2 Me
H
Cl OCHMeCH2 Cl SO2 Me
H
Cl OCH2 CH2 CH2 Cl
SO2 Me
H
Cl OCH2 CH2 Br
SO2 Me
H
Cl Y8 SO2 Me
H
Cl OCH2 CClCH2
SO2 Me
H
Cl OCH2 CClCHCl SO2 Me
H
Cl OCH2 CH2 NO2
SO2 Me
H
Cl OPh SO2 Me
H
Cl OPhMe-2 SO2 Me
H
Cl OPhCl-4 SO2 Me
H
Cl OPhNO2 -4 SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OEt
SO2 Me
H
Cl OCH2 CH2 OPr-n
SO2 Me
H
Cl OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OBu-n
SO2 Me
H
Cl OCH2 CH2 OBu-i
SO2 Me
H
Cl OCH2 CH2 OBu-s
SO2 Me
H
Cl OCH2 CH2 OBu-t
SO2 Me
H
Cl OCH2 CH2Y4
SO2 Me
H
Cl OCHMeCH2 OMe SO2 Me
H
Cl OCH2 CHMeOMe SO2 Me
H
Cl OCH2 CH2 OPh
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
Cl OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
Cl OCH2 CH2 OH
SO2 Me
H
Cl OCH2 Ph SO2 Me
H
Cl OCHMePh SO2 Me
H
Cl OCH2 CH2 Ph
SO2 Me
H
Cl OCH2 Ph-2-Cl SO2 Me
H
Cl OCH2 Ph-3-Me SO2 Me
H
Cl OCH2 Ph-4-OMe SO2 Me
H
Cl OCH2 Ph-4-NO2
SO2 Me
H
Cl Y9 SO2 Me
H
Cl Y10 SO2 Me
H
Cl Y11 SO2 Me
H
Cl Y12 SO2 Me
H
Cl Y13 SO2 Me
H
Cl Y14 SO2 Me
H
Cl Y15 SO2 Me
H
Cl Y16 SO2 Me
H
Cl Y17 SO2 Me
H
Cl Y18 SO2 Me
H
Cl OCH2 CH2 NH2
SO2 Me
H
Cl OCH2 CH2 NHMe
SO2 Me
H
Cl OCH2 CH2 NHPr-i
SO2 Me
H
Cl OCH2 CH2 NMe2
SO2 Me
H
Cl OCH2 CH2 NEt2
SO2 Me
H
Cl Y19 SO2 Me
H
Cl OCH2 COOMe SO2 Me
H
Cl OCH2 COOEt SO2 Me
H
Cl OCH2 COOPr-i SO2 Me
H
Cl OCH2 COOBu-i SO2 Me
H
Cl OCH2 COOBu-t SO2 Me
H
Cl OCH2 COO-Y4 SO2 Me
H
Cl OCHMeCOOMe SO2 Me
H
Cl OCHMeCOOEt SO2 Me
H
Cl OCHMeCOOPr-i SO2 Me
H
Cl OCH2 CH2 CN
SO2 Me
H
Cl OCH2 SMe SO2 Me
H
Cl OCH2 CH2 SMe
SO2 Me
H
Cl OCH2 CH2 S(O)Me
SO2 Me
H
Cl OCH2 CH2 SO2 Me
SO2 Me
H
Cl OCH2 CH2 SPr-i
SO2 Me
H
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
H
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
H
Cl OCOOMe SO2 Me
H
Cl OCOOPr-i SO2 Me
H
Cl OCONH2 SO2 Me
H
Cl OCONHMe SO2 Me
H
Cl OCONMe2 SO2 Me
H
Cl OP(O)(OMe)2 SO2 Me
H
Cl Y20 SO2 Me
H
Cl SCH2 CHCH2
SO2 Me
H
Cl SCH2 CHCMe2
SO2 Me
H
Cl SCH2 C CH SO2 Me
H
Cl SCH2 CF3 SO2 Me
H
Cl SCH2 CCl3
SO2 Me
H
Cl Y21 SO2 Me
H
Cl SPh SO2 Me
H
Cl SCH2 CH2 OMe
SO2 Me
H
Cl SCH2 CH2 OEt
SO2 Me
H
Cl SCH2 CH2 OPr-i
SO2 Me
H
Cl Y22 SO2 Me
H
Cl S(O)CH2 CHCH2
SO2 Me
H
Cl S(O)CH2 CHCMe2
SO2 Me
H
Cl S(O)CH2 CH2 Cl
SO2 Me
H
Cl Y23 SO2 Me
H
Cl SO2 CH2 CHCH2
SO2 Me
H
Cl SO2 CH2 CHCMe2
SO2 Me
H
Cl SO2 CH2 CCH
SO2 Me
H
Cl SO2 CH2 CF3
SO2 Me
H
Cl SO2 CH2 CH2 Cl
SO2 Me
H
Cl Y24 SO2 Me
H
Cl Y25 SO2 Me
H
Cl SO2 Ph SO2 Me
H
Cl SO2 CH2 CH2 OMe
SO2 Me
H
Cl SO2 CH2 CH2 OEt
SO2 Me
H
Cl SO2 CH2 CH2 OPr-i
SO2 Me
H
Cl OCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 OEt
SO2 Me
CH2 Ph
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCHMeCH2 OMe SO2 Me
CH2 Ph
Cl OCH2 CH2 SMe
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
Cl SCH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
Cl OCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SOMe
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
Cl OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
Cl SCH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
Cl SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
Cl OCH2 CH2 OMe
Cl H
Cl OCH2 CH2 OEt
Cl H
Cl OCH2 CH2 OPr-i
Cl H
Cl OCHMeCH2 OMe Cl H
Cl OCH2 COOMe Cl H
Cl OCH2 CH2 SMe
Cl H
Cl OCH2 CH2 SO2 Me
Cl H
Cl SCH2 CH2 OMe
Cl H
Cl SO2 CH2 CH2 OMe
Cl H
Cl OCH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 SMe
Cl CH2 Ph
Cl OCH2 CH2 SOMe
Cl CH2 Ph
Cl OCH2 CH2 SO2 Me
Cl CH2 Ph
Cl SCH2 CH2 OMe
Cl CH2 Ph
Cl SO2 CH2 CH2 OMe
Cl CH2 Ph
Cl OCH2 CH2 OMe
Cl CH2 COPh
Cl OCH2 CH2 SMe
Cl CH2 COPh
Cl OCH2 CH2 SO2 Me
Cl CH2 COPh
Cl SCH2 CH2 OMe
Cl CH2 COPh
Cl SCH2 CH2 OEt
Cl CH2 COPh
Cl SO2 CH2 CH2 OMe
Cl CH2 COPh
OMe Y1 SO2 Me
H
OMe Y2 SO2 Me
H
OMe Y3 SO2 Me
H
OMe Y4 SO2 Me
H
OMe Y5 SO2 Me
H
OMe Y6 SO2 Me
H
OMe Y7 SO2 Me
H
OMe OCH2 CHCH2
SO2 Me
H
OMe OCHMeCHCH2 SO 2 Me
H
OMe OCMe2 CHCH2
SO2 Me
H
OMe OCH2 CMeCH2
SO2 Me
H
OMe OCH2 CHCHMe SO2 Me
H
OMe OCH2 CHCMe2
SO2 Me
H
OMe OCH2 CH2 CHCH2
SO2 Me
H
OMe OCH2 CCH SO2 Me
H
OMe OCHMeCCH SO2 Me
H
OMe OCMe2 CCH SO2 Me
H
OMe OCH2 CCMe SO2 Me
H
OMe OCH2 CH2 F
SO2 Me
H
OMe OCH2 CHF2
SO2 Me
H
OMe OCH2 CF3 SO2 Me
H
OMe OCH2 CH2 Cl
SO2 Me
H
OMe OCH2 CCl3
SO2 Me
H
OMe OCHMeCH2 Cl SO2 Me
H
OMe OCH2 CH2 CH2 Cl
SO2 Me
H
OMe OCH2 CH2 Br
SO2 Me
H
OMe Y8 SO 2 Me
H
OMe OCH2 CClCH2
SO2 Me
H
OMe OCH2 CClCHCl SO2 Me
H
OMe OCH2 CH2 NO2
SO2 Me
H
OMe OPh SO2 Me
H
OMe OPhMe-2 SO2 Me
H
OMe OPhCl-4 SO2 Me
H
OMe OPhNO2 -4 SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OEt
SO2 Me
H
OMe OCH2 CH2 OPr-n
SO2 Me
H
OMe OCH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OBu-n
SO2 Me
H
OMe OCH2 CH2 OBu-i
SO2 Me
H
OMe OCH2 CH2 OBu-s
SO2 Me
H
OMe OCH2 CH2 OBu-t
SO2 Me
H
OMe OCH2 CH2Y4
SO2 Me
H
OMe OCHMeCH2 OMe SO2 Me
H
OMe OCH2 CHMeOMe SO2 Me
H
OMe OCH2 CH2 OPh
SO2 Me
H
OMe OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
OMe OCH2 CH2 OCH2 CH 2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
OMe OCH2 CH2 OH
SO2 Me
H
OMe OCH2 Ph SO2 Me
H
OMe OCHMePh SO2 Me
H
OMe OCH2 CH2 Ph
SO2 Me
H
OMe OCH2 Ph-2-Cl SO2 Me
H
OMe OCH2 Ph-3-Me SO2 Me
H
OMe OCH2 Ph-4-OMe SO2 Me
H
OMe OCH2 Ph-4-NO2
SO2 Me
H
OMe Y9 SO2 Me
H
OMe Y10 SO2 Me
H
OMe Y11 SO2 Me
H
OMe Y12 SO2 Me
H
OMe Y13 SO2 Me
H
OMe Y14 SO2 Me
H
OMe Y15 SO2 Me
H
OMe Y16 SO2 Me
H
OMe Y17 SO2 Me
H
OMe Y18 SO2 Me
H
OMe OCH2 CH2 NH2
SO2 Me
H
OMe OCH2 CH2 NHMe
SO2 Me
H
OMe OCH2 CH2 NHPr-i
SO2 Me
H
OMe OCH2 CH2 NMe2
SO2 Me
H
OMe OCH2 CH2 NEt2
SO2 Me
H
OMe Y19 SO2 Me
H
OMe OCH2 COOMe SO2 Me
H
OMe OCH2 COOEt SO2 Me
H
OMe OCH2 COOPr-i SO2 Me
H
OMe OCH2 COOBu-i SO2 Me
H
OMe OCH2 COOBu-t SO2 Me
H
OMe OCH2 COOY4 SO2 Me
H
OMe OCHMeCOOMe SO2 Me
H
OMe OCHMeCOOEt SO2 Me
H
OMe OCHMeCOOPr-i SO2 Me
H
OMe OCH2 CH2 CN
SO2 Me
H
OMe OCH2 SMe SO2 Me
H
OMe OCH2 CH2 SMe
SO2 Me
H
OMe OCH2 CH2 S(O)Me
SO2 Me
H
OMe OCH2 CH2 SO2 Me
SO2 Me
H
OMe OCH2 CH2 SPr-i
SO2 Me
H
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
H
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
H
OMe OCOOMe SO2 Me
H
OMe OCOOPr-i SO2 Me
H
OMe OCONH2 SO2 Me
H
OMe OCONHMe SO2 Me
H
OMe OCONME2 SO2 Me
H
OMe OP(O)(OMe)2 SO2 Me
H
OMe Y20 SO2 Me
H
OMe SCH 2 CHCH2
SO2 Me
H
OMe SCH2 CHCMe2
SO2 Me
H
OMe SCH2 CCH SO2 Me
H
OMe SCH2 CF3 SO2 Me
H
OMe SCH2 CCl3
SO2 Me
H
OMe Y21 SO2 Me
H
OMe SPh SO2 Me
H
OMe SCH2 CH2 OMe
SO2 Me
H
OMe SCH2 CH2 OEt
SO2 Me
H
OMe SCH2 CH2 OPr-i
SO2 Me
H
OMe Y22 SO2 Me
H
OMe S(O)CH2 CHCH2
SO2 Me
H
OMe S(O)CH2 CHCMe2
SO2 Me
H
OMe S(O)CH2 CCH SO2 Me
H
OMe S(O)CH2 CH2 Cl
SO2 Me
H
OMe Y23 SO2 Me
H
OMe SO2 CH2 CHCH2
SO2 Me
H
OMe SO2 CH2 CHCMe2
SO2 Me
H
OMe SO2 CH2 CCH
SO2 Me
H
OMe SO2 CH2 CF3
SO2 Me
H
OMe SO2 CH2 CH2 Cl
SO2 Me
H
OMe Y24 SO2 Me
H
OMe Y25 SO2 Me
H
OMe SO2 Ph SO2 Me
H
OMe SO2 CH2 CH2 OMe
SO2 Me
H
OMe SO2 CH2 CH2 OEt
SO2 Me
H
OMe SO2 CH2 CH2 OPr-i
SO2 Me
H
OMe OCH2 CH2 OMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 OEt
SO2 Me
CH2 Ph
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCHMeCH2 OMe SO2 Me
CH2 Ph
OMe OCH2 CH2 SMe
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
OMe SCH 2 CH2 OMe
SO2 Me
CH2 Ph
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
OMe OCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SOMe
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
OMe OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
OMe SCH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
OMe SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
OMe OCH2 CH2 OMe
Cl H
OMe OCH 2 CH2 OEt
Cl H
OMe OCH2 CH2 OPr-i
Cl H
OMe OCHMeCH2 OMe Cl H
OMe OCH2 COOMe Cl H
OMe OCH2 CH2 SMe
Cl H
OMe OCH2 CH2 SO2 Me
Cl H
OMe SCH2 CH2 OMe
Cl H
OMe SO2 CH2 CH2 OMe
Cl H
OMe OCH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 SMe
Cl CH2 Ph
OMe OCH2 CH2 SOMe
Cl CH2 Ph
OMe OCH2 CH2 SO2 Me
Cl CH2 Ph
OMe SCH2 CH2 OMe
Cl CH2 Ph
OMe SO2 CH2 CH2 OMe
Cl CH2 Ph
OMe OCH2 CH2 OMe
Cl CH2 COPh
OMe OCH2 CH2 SMe
Cl CH2 COPh
OMe OCH2 CH2 SO2 Me
Cl CH2 COPh
OMe SCH2 CH2 OMe
Cl CH2 COPh
OMe SCH2 CH2 OEt
Cl CH2 COPh
OMe SO2 CH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
Y1 SO2 Me
H
CH2 OMe
Y2 SO2 Me
H
CH2 OMe
Y3 SO2 Me
H
CH2 OMe
Y4 SO2 Me
H
CH2 OMe
Y5 SO2 Me
H
CH2 OMe
Y6 SO2 Me
H
CH2 OMe
Y7 SO2 Me
H
CH2 OMe
OCH2 CHCH2
SO2 Me
H
CH2 OMe
OCHMeCHCH2 SO2 Me
H
CH2 OMe
OCHMe2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CMeCH2
SO2 Me
H
CH2 OMe
OCH2 CHCHMe SO2 Me
H
CH2 OMe
OCH2 CHCMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 CHCH2
SO2 Me
H
CH2 OMe
OCH2 CCH SO2 Me
H
CH2 OMe
OCHMeCCH SO2 Me
H
CH2 OMe
OCMe2 CCH SO2 Me
H
CH2 OMe
OCH2 CCMe SO 2 Me
H
CH2 OMe
OCH2 CH2 F
SO2 Me
H
CH2 OMe
OCH2 CHF2
SO2 Me
H
CH2 OMe
OCH2 CF3 SO2 Me
H
CH2 OMe
OCH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CCl3
SO2 Me
H
CH2 OMe
OCHMeCH2 Cl SO2 Me
H
CH2 OMe
OCH2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
OCH2 CH2 Br
SO2 Me
H
CH2 OMe
Y8 SO2 Me
H
CH2 OMe
OCH2 CClCH2
SO2 Me
H
CH2 OMe
OCH2 CClCHCl SO2 Me
H
CH2 OMe
OCH2 CH2 NO2
SO2 Me
H
CH2 OMe
OPh SO2 Me
H
CH2 OMe
OPhMe-2 SO2 Me
H
CH2 OMe
OPhCl-4 SO2 Me
H
CH2 OMe
OPhNO2 -4 SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OEt
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-n
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-s
SO2 Me
H
CH2 OMe
OCH2 CH2 OBu-t
SO2 Me
H
CH2 OMe
OCH2 CH2Y4
SO2 Me
H
CH2 OMe
OCHMeCH2 OMe SO2 Me
H
CH2 OMe
OCH2 CHMeOMe SO2 Me
H
CH2 OMe
OCH2 CH2 OPh
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OCHMeCH2 OMe
SO2 Me
H
CH2 OMe
OCH2 CH2 OH
SO2 Me
H
CH2 OMe
OCH2 Ph SO2 Me
H
CH2 OMe
OCHMePh SO2 Me
H
CH2 OMe
OCH2 CH 2 Ph
SO2 Me
H
CH2 OMe
OCH2 Ph-2-Cl SO2 Me
H
CH2 OMe
OCH2 Ph-3-Me SO2 Me
H
CH2 OMe
OCH2 Ph-4-OMe SO2 Me
H
CH2 OMe
OCH2 Ph-4-NO2
SO2 Me
H
CH2 OMe
Y9 SO2 Me
H
CH2 OMe
Y10 SO2 Me
H
CH2 OMe
Y11 SO2 Me
H
CH2 OMe
Y12 SO2 Me
H
CH2 OMe
Y13 SO2 Me
H
CH2 OMe
Y14 SO2 Me
H
CH2 OMe
Y15 SO2 Me
H
CH2 OMe
Y16 SO2 Me
H
CH2 OMe
Y17 SO2 Me
H
CH2 OMe
Y18 SO2 Me
H
CH2 OMe
OCH2 CH2 NH2
SO2 Me
H
CH2 OMe
OCH2 CH2 NHMe
SO2 Me
H
CH2 OMe
OCH2 CH2 NHPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 NMe2
SO2 Me
H
CH2 OMe
OCH2 CH2 NEt2
SO2 Me
H
CH2 OMe
Y19 SO2 Me
H
CH2 OMe
OCH2 COOMe SO2 Me
H
CH2 OMe
OCH2 COOEt SO2 Me
H
CH2 OMe
OCH2 COOPr-i SO2 Me
H
CH2 OMe
OCH2 COOBu-i SO2 Me
H
CH2 OMe
OCH2 COOBu-t SO2 Me
H
CH2 OMe
OCH2 COOY4 SO2 Me
H
CH2 OMe
OCHMeCOOMe SO2 Me
H
CH2 OMe
OCHMeCOOEt SO2 Me
H
CH2 OMe
OCHMeCOOPr-i SO2 Me
H
CH2 OMe
OCH2 CH2 CN
SO2 Me
H
CH2 OMe
OCH2 SMe SO2 Me
H
CH2 OMe
OCH2 CH2 SMe
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
H
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
H
CH2 OMe
OCOOMe SO2 Me
H
CH2 OMe
OCOOPr-i SO2 Me
H
CH2 OMe
OCONH2 SO2 Me
H
CH2 OMe
OCONHME SO2 Me
H
CH2 OMe
OCONMe2 SO2 Me
H
CH2 OMe
OP(O)(OMe)2 SO2 Me
H
CH2 OMe
Y20 SO2 Me
H
CH2 OMe
SCH2 CHCH2
SO2 Me
H
CH2 OMe
SCH2 CHCMe2
SO2 Me
H
CH2 OMe
SCH2 CCH SO2 Me
H
CH2 OMe
SCH2 CF3 SO2 Me
H
CH2 OMe
SCH2 CCl3
SO2 Me
H
CH2 OMe
Y21 SO2 Me
H
CH2 OMe
SPh SO2 Me
H
CH2 OMe
SCH2 CH2 OMe
SO2 Me
H
CH2 OMe
SCH2 CH2 OEt
SO2 Me
H
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
Y22 SO2 Me
H
CH2 OMe
S(O)CH2 CHCH2
SO2 Me
H
CH2 OMe
S(O)CH2 CHCMe2
SO2 Me
H
CH2 OMe
S(O)CH2 C CH SO2 Me
H
CH2 OMe
S(O)CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y23 SO2 Me
H
CH2 OMe
SO2 CH2 CHCH2
SO2 Me
H
CH2 OMe
SO2 CH2 CHCMe2
SO2 Me
H
CH2 OMe
SO2 CH2 CCH
SO2 Me
H
CH2 OMe
SO2 CH2 CF3
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 Cl
SO2 Me
H
CH2 OMe
Y24 SO2 Me
H
CH2 OMe
SO2 Ph SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OEt
SO2 Me
H
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
H
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OEt
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCHMeCH2 OMe SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 S(O)Pr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 Ph
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 Ph
CH2 OMe
OCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SOMe
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Pr-i
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SCH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
SO2 Me
CH2 COPh
CH2 OMe
SO2 CH2 CH2 OPr-i
SO2 Me
CH2 COPh
CH2 OMe
OCH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OEt
Cl H
CH2 OMe
OCH2 CH2 OPr-i
Cl H
CH2 OMe
OCHMeCH2 OMe Cl H
CH2 OMe
OCH2 COOMe Cl H
CH2 OMe
OCH2 CH2 SMe
Cl H
CH2 OMe
OCH2 CH2 SO2 Me
Cl H
CH 2 OMe
SCH2 CH2 OMe
Cl H
CH2 OMe
SO2 CH2 CH2 OMe
Cl H
CH2 OMe
OCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SOMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 Ph
CH2 OMe
SCH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 Ph
CH2 OMe
OCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SMe
Cl CH2 COPh
CH2 OMe
OCH2 CH2 SO2 Me
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OMe
Cl CH2 COPh
CH2 OMe
SCH2 CH2 OEt
Cl CH2 COPh
CH2 OMe
SO2 CH2 CH2 OMe
Cl CH2 COPh
______________________________________

When the compound of the present invention is to be used as an agricultural or horticultural herbicide, it is usually mixed with a suitable carrier, for instance, a solid carrier such as clay, talc, bentonite or diatomaceous earth, or a liquid carrier such as water, an alcohol (such as benzene, toluene or xylene), a chlorinated hydrocarbon, an ether, a ketone, an ester (such as ethyl acetate) or an acid amide (such as dimethylformamide). If desired, an emulsifier, a dispersing agent, a suspending agent, a penetrating agent, a spreader or a stabilizer may be added to prepare an optional formulation such as a liquid formulation, an emulsifiable concentrate, a wettable powder, a dust, a granule or a flowable.

Further, if desired, other herbicides, various insecticides, bacteriocides, plant regulating agents or synergism agents may be combined at the time of the preparation of the formulations or at the time of the application of the herbicides.

As other herbicides to be combined with the herbicide of the present invention, there may be mentioned, for instance, compounds disclosed in Farm Chemicals Handbook, the 73rd Edition (1987). Among them, there may be mentioned, for example, atrazine, cyanazine, alachlor, metolachlor, EPTC, 2,4-D, butylate, dicamba, bromoxynil, tridiphane, isoproturon, chlortoluron, triallate, difluphenican, diclofop methyl, diphenzoquat, imazamethabenz methyl, ioxynil, methabenzthazuron, fluroxypil, chlorsulfuron and N-[(4,6-di(difluoromethoxy)pyrimidin-2-yl)aminocarbonyl]-2-methoxycarbonyl benzenesulfonamide. N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]-3-chloro-4-methoxycarbonyl -1-methylpyrazole-5-sulfonamide or N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-3-bromo-4-methoxycarbonyl-1 -methylpyrazole-5sulfonamide as disclosed in U.S. Pat. No. 4,668,277, or N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-3-dimethylaminocarbonylpyri dine-2-sulfonamide as disclosed in Japanese Unexamined Patent Publication No. 223180/1987 may also be combined with the herbicide of the present invention.

The dose varies depending upon the application site, the season for application, the method for application, the type of the crop plant, etc. In general, however, the dose is usually within a range of from 0.001 to 10 kg per hectare as the amount of the active ingredient.

Now, Formulation Examples of the herbicides containing the compounds of the present inveniton as active ingredients, will be given. However, it should be understood that the present invention is by no means restricted to such specific Examples. In the following Formulation Examples, "parts" means "parts by weight".

FORMULATION EXAMPLE 1
PAC Wettable powder
______________________________________
Compound No. 1 of the present invention
60 parts
Zeeklite PFP (tradename for a kaolin-type
33 parts
clay, manufactured by Zeeklite Industries,
Co., Ltd.)
Sorpol 5039 (tradename for a mixture of a
5 parts
nonionic surfactant and an anionic
surfactant, manufactured by Toho Chemical
Co., Ltd.)
Carplex (tradename for a coagulation-
2 parts
preventing agent composed of a mixture of a
surfactant and fine silica powder,
manufactured by Shionogi Pharmaceutical
Co., Ltd.)
______________________________________

The above ingredients are homogeneously pulverized and mixed to form a wettable powder.

FORMULATION EXAMPLE 2
PAC Emulsifiable concentrate
______________________________________
Compound No. 1 of the present invention
1.5 parts
Xylene 78.5 parts
N,N-dimethylformamide 15 parts
Sorpol 2680 (tradename for a mixture of a
5 parts
nonionic surfactant and an anionic
surfactant, manufactured by Toho Chemical
Co., Ltd.)
______________________________________

The above ingredients are homogeneously mixed to form an emulsifiable concentrate.

FORMULATION EXAMPLE 3
PAC Flowable
______________________________________
Compound No. 1 of the present invention
40 parts
Agrizole B-710 (tradename for a nonionic
10 parts
surfactant, manufactured by Kao
Corporation)
Runox 1000C (tradename for an anionic
0.5 part
surfactant, manufactured by Toho Chemical
Co., Ltd.)
1% Rodopol water (tradename for a thickner,
20 parts
manufactured by Rhone-Poulenc)
Water 29.5 parts
______________________________________

The above ingredients are homogeneously mixed to form a flowable.

FORMULATION EXAMPLE 4
PAC Liquid formulation
______________________________________
Sodium salt of Compound No 1 of the
30 parts
present invention
Nippol (tradename for a nonionic
10 parts
surfactant, manufactured by Nissan
Chemical Industries Ltd.)
Water 60 parts
______________________________________

The above ingredients are homogeneously mixed to obtain a liquid formulation.

FORMULATION EXAMPLE 5
PAC Liquid formulation
______________________________________
Potassium salt of Compound No. 1 of the
30 parts
present invention
Nippol (tradename for a nonionic
10 parts
surfactant, manufactured by Nissan
Chemical Industries Ltd.)
Water 60 parts
______________________________________

The above ingredients are homogeneously mixed to obtain a liquid formulation.

FORMULATION EXAMPLE 6
PAC Liquid formulation
______________________________________
Calcium salt of Compound No. 1 of the
30 parts
present invention
Nippol (tradename for a nonionic
10 parts
surfactant, manufactured by Nissan
Chemical Industries Ltd.)
Water 60 parts
______________________________________

The above ingredients are homogeneously mixed to obtain a liquid formulation.

FORMULATION EXAMPLE 7
PAC Liquid formulation
______________________________________
Isopropylamine salt of Compound No. 1 of the
10 parts
present invention
Sorpol W-150 (tradename for a nonionic
10 parts
surfactant, manufactured by Toho Chemical
Co., Ltd.)
Water 80 parts
______________________________________

The above ingredients are homogeneously mixed to form a liquid formulation.

In their use, the above wettable powder, emulsifiable concentrates, flowables or liquid formulations are diluted with water from 50 to 1,000 times and applied so that the respective active ingredients will be from 0.001 to 5 kg per hectare.

The compounds of the present invention are applicable not only to agricultural and horticultural fields such as upland fields, paddy fields and orchards, but also to non-agricultural fields such as athletic fields, vacant fields and railway sides for the control of various weeds. The dose in their application varies depending upon the application site, the season for application, the type of crop plants, etc. However, it is usually within a range of from 0.001 to 5 kg per hectare.

Now, the herbicidal activities of the compounds of the present invention will be described with respect to specific Test Examples.

TEST EXAMPLE 1:
PAC Test on the herbicidal effects in soil treatment

A plastic box having a length of 15 cm, a width of 22 cm and a depth of 6 cm was filled with a sterilized diluvium soil, and seeds of Echinochloa crus-galli, Setaria viridis, Eleusine indica, Digitaria adscendens, Panicum dichotomiflorum, Abutilon theophrasti, Amaranthus lividus, Polygonum longisetum and Zea mays were sown, and tubers of Cyperus esculentus were further planted. The soil was covered thereon in the thickness of about 1.5 cm, and then a herbicide solution was applied onto the surface of the soil uniformly so that the active ingredient was distributed at a predetermined concentration. The herbicide solution was prepared by diluting the wettable powder, the emulsifiable concentrate, the liquid formulation or the flowable as described in the foregoing Formulation Examples with water and applied onto the entire soil surface by means of a small spray. Three weeks after the application of the herbicidal solution, the herbicidal effects against each weed were determined on the basis of the following standard ratings. The results thereby obtained are shown in Table 9. The Compound Nos. correspond to the Compound Nos. in Table 2.

Standard ratings

5: Growth control rate of more than 90% (almost completely withered)

4: Growth control rate of from 70 to 90%

3: Growth control rate of from 40 to 70%

2: Growth control rate of from 20 to 40%

1: Growth control rate of from 5 to 20%

0: Growth control rate of less than 5% (almost non-effective)

The above growth control rates were calculated by the following equation: ##EQU1## where T: Weight of the weed growth above the soil surface of the treated area

N: Weight of the weed growth above the soil surface of the non-treated area

TEST EXAMPLE 2:
PAC Test 1 on the herbicidal effects in foliage treatment

A plastic box having a length of 15 cm, a width of 22 cm and a depth of 6 cm was filled with a sterilized diluvium soil, and seeds of Echinochloa crus-galli, Setaria viridis, Eleusine indica, Digitaria adscendens, Panicum dichotomiflorum, Xanthium strumatirum, Abutilon theophrasti, Amaranthus lividus, Polygonum longisetum and Zea mays were spot-wisely sown, and tubers of Cyperus esculentus were further planted. Then, the soil was covered thereon in a thickness of about 1.5 cm. When the various weeds and crop plant grew to the 2 or 3 leaf stage, a herbicidal solution was uniformly sprayed on the foliages so that the active ingredient was applied in a predetermined concentration.

The herbicidal solution was prepared by diluting the wettable powder, the emulsifiable concentrate, the liquid formulation or the flowable as described in the above Formulation Examples with water and applied onto the entire surface of the foliages of the weeds and the crop plants by a small spray. Two weeks after the application of the herbicide solution, the herbicidal effects against each weed and Zea mays were determined on the basis of the standard ratings described in Test Example 1. The results are shown in Table 10. The Compound Nos. in Table 10 correspond to the Compound Nos. in Table 2.

TEST EXAMPLE 3
PAC Test 2 on the herbicidal effects in foliage treatment

A plastic box having a length of 15 cm, a width of 22 cm and a depth of 6 cm was filled with a sterilized diluvium soil, and seeds of Veronica persica, Stellaria media, Galium spurium, Matricaria matricarioides, Polygonum persicaria, Lamium purpureum, Solanum nigrum and Triticum aestivum were spot-wisely sown. Then, the soil was covered thereon in a thickness of about 1.5 cm. When the various weeds and crop plant grew to the 2 or 3 leaf atage, a herbicidal solution was uniformly sprayed on the foliages so that the active ingredient was applied in a predetermined concentration.

The herbicidal solution was prepared by diluting the wettable powder, the emulsifiable concentrate, the liquid formulation or the flowable as described in the above Formulation Examples with water and applied onto the entire surface of the foliages of the weeds and Triticum aestivum by a small spray. Two weeks after the application of the herbicide solution, the herbicidal effects against each weed and Triticum aestivum were determined on the basis of the standard ratings described in Test Example 1 The results are shown in Table 11. The Compound Nos in Table 11 correspond to Compound Nos. in Table 2.

In Tables 9, 10 and 11, the following abbreviations are used.

Dose: Dose of active ingredient (g/are)

EC: Echinochloa crus-galli (barnyardgrass)

SE: Setaria viridis (green foxtail)

EL: Eleusine indica (goosegrass)

DI: Digitaria adscendens (large crabgrass)

PA: Panicum dichotomiflorum (fall panicum)

AB: Abutilon theophrasti (velvet leaf)

AM: Amaranthus lividus (livid amaranth)

PO: Polygonum longisetum (persicaria blumei gross)

XA: Xanthium strumarium (cocklebur)

CY: Cyperus esculentus (yellow nutsedge)

ZE: Zea mays (corn)

VE: Veronica persia (birdseye speedweell)

ST: Stellaria media (chickweed)

GA: Galium spurium (catchweed)

MA: Matricaria matricarioides (pineappleweed)

PP: Polygonum persicaria (ladysthumb)

LA: Lamium purpureum (red deadnettle)

SO: Solanum nigrum (black nigthshade)

TR: Triticum aestivum (wheat)

TABLE 9
__________________________________________________________________________
Compound
Dose
No. g/are
EC SE
EL DI
PA AB AM PO CY ZE
__________________________________________________________________________
1 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
4 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
6 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
7 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
11 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
18 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
19 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
20 1 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 0
Compara-
4 3 1 3 3 1 4 5 5 0 0
tive 8 4 2 4 4 2 5 5 5 0 0
Compound
16 5 3 5 5 3 5 5 5 1 1
Compara-
4 5 5 5 5 5 1 1 1 2 0
tive 8 5 5 5 5 5 2 2 2 3 0
Compound
16 5 5 5 5 5 3 3 3 4 1
B
__________________________________________________________________________
TABLE 10
__________________________________________________________________________
Compound
Dose
No. g/are
EC SE
EL DI
PA AB AM PO XA CY ZE
__________________________________________________________________________
1 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
4 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
6 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
7 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
11 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
18 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
19 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
20 1 5 5 5 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 5 5 5 0
4 5 5 5 5 5 5 5 5 5 5 0
Compara-
4 3 1 2 3 0 3 5 5 4 0 0
tive 8 4 2 3 4 1 5 5 5 5 0 1
Compound
16 4 2 3 4 1 5 5 5 5 0 1
Compara-
4 4 3 3 4 3 0 2 2 0 1 0
tive 8 4 4 4 4 4 1 3 3 1 2 1
Compound
16 5 5 5 5 5 2 4 4 2 3 2
B
__________________________________________________________________________
TABLE 11
______________________________________
Com-
pound Dose
No. g/are VE ST GA MA PP LA SO TR
______________________________________
1 0.5 5 5 5 5 5 5 5 0
1 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 0
7 0.5 5 5 5 5 5 5 5 0
1 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 0
11 0.5 5 5 5 5 5 5 5 0
1 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 0
18 0.5 5 5 5 5 5 5 5 0
1 5 5 5 5 5 5 5 0
2 5 5 5 5 5 5 5 0
Compar-
1 4 4 3 2 4 2 4 0
ative 2 5 5 4 4 5 4 5 1
Com-
pound C
______________________________________

In Tables 9 and 10, the Comparative Compounds are as follows: ##STR40##

In Table 11, the Comparative Compound is as follows:

INVENTORS:

Suzuki, Koichi, Oya, Eiichi, Nawamaki, Tsutomu, Watanabe, Shigeomi, Watanabe, Junichi, Kondo, Yasuo, Kakuta, Takuya

THIS PATENT IS REFERENCED BY THESE PATENTS:
Patent Priority Assignee Title
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5824802, Mar 24 1998 Dow Agrosciences LLC 1-alkyl-4-benzoyl-5-hydroxypyrazole compounds and their use as herbicides
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