US2017015649A1PendingUtilityA1
N-Thio-anthranilamid compounds and their use as pesticides
Est. expiryJul 7, 2025(expired)· nominal 20-yr term from priority
Inventors:Thomas SchmidtMichael PuhlJoachim DickhautHenricus Maria Martinus BastiaansMichael RackDeborah L. CulbertsonDouglas D. AnspaughFranz-Josef BraunToni BucciHenry Van Tuyl CotterDavid G. KuhnHassan Oloumi-Sadeghi
A61P 33/00C07D 413/14A01N 43/84C07D 409/14C07D 401/04C07D 401/14A01N 43/56
59
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Claims
Abstract
N-Thio-anthranilamid compounds of formula (I) wherein A is A 1 wherein the variables and the indices are as defined per the description, processes for preparing the compounds I, pesticidal compositions comprising compounds I, use of compounds I for the control of insects, acarids or nematodes, and methods for treating, controlling, preventing or protecting animals against infestation or infection by parasites by use of compounds of formula I.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 : A compound of formula (I)
wherein
R 1 is hydrogen;
A is A 1
wherein
# denotes the binding site;
R 2 and R 3 each independently are R 6 , or
R 2 and R 3 together with the sulfur atom to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, which ring can be fused with one or two saturated, partially unsaturated or unsaturated 5- to 6-membered rings which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of the above rings are unsubstituted or substituted by any combination of 1 to 6 groups R 8 ;
G is oxygen or sulfur;
R 6 is C 1 -C 20 -alkyl, C 2 -C 20 -alkenyl, C 2 -C 20 -alkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -cycloalkenyl, C 3 -C 8 -cycloalkynyl, phenyl, naphthyl, biphenyl, or a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein all of these groups are unsubstituted or substituted by any combination of 1 to 6 groups R 8 ;
R 8 is R 9 ; or two groups R 8 together with the atoms to which they are attached form a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which may contain 1 to 4 heteroatoms/heterogroups selected from oxygen, nitrogen, sulfur, SO and SO 2 , and which ring system is unsubstituted or substituted with any combination of 1 to 6 groups R 9 .
R 9 is R 10 , R 11 , —C(=G)R 10 , —C(═NOR 10 )R 10 , —C(═NNR 10 2 )R 10 , —C(=G)OR 10 , —C(=G)NR 10 2 , —OC(=G)R 10 , —OC(=G)OR 10 , —NR 10 C(=G)R 10 , —N[C(=G)R 10 ]2, —NR 10 C(=G)OR 10 , —C(=G)NR 10 —NR 10 2 , —C(=G)NR 10 —NR 10 [C(=G)R 10 ], —NR 10 —C(=G)NR 10 2 , —NR 10 —NR 10 C(=G)R 10 , —NR 10 —N[C(=G)R 10 ] 2 , —N[(C=G)R 10 ]—NR 10 2 , —NR 10 —NR 10 [(C=G)GR 10 ], —NR 10 [(C=G)NR 10 2 , —NR 10 [C═NR 10 ]R 10 , —NR 10 (C═NR 10 )NR 10 2 , —O—NR 10 2 , —O—NR 10 (C=G)R 10 , —SO 2 NR 10 2 , —NR 10 SO 2 R 10 , —SO 2 OR 10 , —OSO2R 10 , —OR 10 , —NR 10 2 , —SiR 10 3 , —PR 10 2 , —P(=G)R 10 , —SOR 10 , —SO 2 R 10 , —PG 2 R 10 2 , —PG 3 R 10 2 or two groups R 9 together are (=G),)(═N—R 10 ), (═CR 10 2 ), (═CHR 10 ), or (═CH 2 );
R 10 is C 1 -C 10 , C 2 -C 10 -alkenyl, C 2 -C 10 -alkynyl, C 3 -C 8 -cycloalkyl, C 4 -C 8 -cycloalkenyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, C 4 -C 8 -cycloalkenyl-C 1 -C 4 -alkyl, C 3 -C 8 -cycloalkyl-C 2 -C 4 -alkenyl, C 4 -C 8 -cycloalkenyl-C 2 -C 4 -alkenyl, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkyl, C 2 -C 10 -alkenyl-C 3 -C 8 -cycloalkyl, C 2 -C 10 -alkynyl-C 3 -C 8 -cycloalkyl, C 1 -C 10 -alkyl-C 4 -C 8 -cycloalkenyl, C 2 -C 10 -alkenyl-C 4 -C 8 -cycloalkenyl, C 2 -C 10 -alkynyl-C 4 -C 8 -cycloalkenyl,
a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sufur, wherein the above groups are unsubstituted or substituted with any combination of from 1 to 6 groups R 11 ;
R 11 is halogen, cyano, nitro, hydroxy, mercapto, amino, formyl, C 1 -C 10 -alkylcarbonyl, C 1 -C 10 -alkoxy, C 2 -C 10 -alkenyloxy, C 2 -C 10 -alkynyloxy, C 1 -C 10 -haloalkoxy, C 3 -C 10 -haloalkenyloxy, C 3 -C 10 -haloalkynyloxy, C 3 -C 8 -cycloalkoxy, C 4 -C 8 -cycloalkenyloxy, C 3 -C 8 -halocycloalkoxy, C 4 -C 8 -halocycloalkenyloxy, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkoxy, C 4 -C 8 -cycloalkenyl-C 1 -C 4 -alkoxy, C 3 -C 8 -cycloalkyl-C 2 -C 4 -alkenyloxy, C 4 -C 8 -cycloalkenyl-C 2 -C 4 -alkenyloxy, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkoxy, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkoxy, C 1 -C 10 -alkynyl-C 3 -C 8 -cycloalkoxy, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkenyloxy, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkenyloxy, C 1 -C 4 -alkoxy-C 1 -C 10 -alkoxy, C 1 -C 4 -alkoxy-C 2 -C 10 -alkenyloxy, mono- or di(C 1 -C 10 -alkyl)carbamoyl, mono- or di(C 1 -C 10 -haloalkyl)carbamoyl, mono- or di(C 3 -C 8 -cycloalkyl)carbamoyl,
C 1 -C 10 -alkoxycarbonyl, C 3 -C 8 -cycloalkoxycarbonyl, C 1 -C 10 -alkylcarbonyloxy, C 3 -C 8 -cyclo alkylcarbonyloxy, C 1 -C 10 -haloalkoxycarbonyl, C 1 -C 10 -haloalkylcarbonyloxy, C 1 -C 10 -alkanamido, C 1 -C 10 -haloalkanamido, C 2 -C 10 -alkenamido, C 3 -C 8 -cycloalkanamido, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkanamido, C 1 -C 10 -alkylthio, C 2 -C 10 -alkenylthio, C 2 -C 10 -alkynylthio, C 1 -C 10 -haloalkylthio, C 2 -C 10 -haloalkenylthio, C 2 -C 10 -haloalkynylthio, C 3 -C 8 -cycloalkylthio, C 3 -C 8 -cycloalkenylthio, C 3 -C 8 -halocycloalkylthio, C 3 -C 8 -halocycloalkenylthio, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkylthio, C 4 -C 8 -cycloalkenyl-C 1 -C 4 -alkylthio, C 3 -C 8 -cycloalkyl-C 2 -C 4 -alkenylthio, C 4 -C 8 -cycloalkenyl-C 2 -C 4 -alkenylthio, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkylthio, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkylthio, C 1 -C 10 -alkynyl-C 3 -C 8 -cycloalkylthio, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkenylthio, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkenylthio, C 1 -C 10 -alkylsulfinyl, C 2 -C 10 -alkenylsulfinyl, C 2 -C 10 -alkynylsulfinyl, C 1 -C 10 -haloalkylsulfinyl, C 2 -C 10 -haloalkenylsulfinyl, C 2 -C 10 -haloalkynylsulfinyl, C 3 -C 8 -cycloalkylsulfinyl, C 3 -C 8 -cycloalkenylsulfinyl, C 3 -C 8 -halocycloalkylsulfinyl, C 3 -C 8 -halocycloalkenylsulfinyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkylsulfinyl, C 4 -C 8 -cycloalkenyl-C 1 -C 4 -alkylsulfinyl, C 3 -C 8 -cycloalkyl-C 2 -C 4 -alkenylsulfinyl, C 4 -C 8 -cycloalkenyl-C 2 -C 4 -alkenylsulfinyl, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkylsulfinyl, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkylsulfinyl, C 1 -C 10 -alkynyl-C 3 -C 8 -cycloalkylsulfinyl, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkenylsulfinyl, C 3 -C 8 -cycloalkenylsulfinyl, C 1 -C 10 -alkylsulfonyl, C 2 -C 10 -alkenylsulfonyl, C 2 -C 10 -alkynylsulfonyl, C 1 -C 10 -haloalkylsulfonyl, C 2 -C 10 -haloalkenylsulfonyl, C 2 -C 10 -haloalkynylsulfonyl, C 3 -C 8 -cycloalkylsulfonyl, C 3 -C 8 -cycloalkenylsulfonyl, C 3 -C 8 -halocycloalkylsulfonyl, C 3 -C 8 -halocycloalkenylsulfonyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkylsulfonyl, C 4 -C 8 -cycloalkenyl-C 1 -C 4 -alkylsulfonyl, C 3 -C 8 -cycloalkyl-C 2 -C 4 -alkenylsulfonyl, C 4 -C 8 -cycloalkenyl-C 2 -C 4 -alkenylsulfonyl, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkylsulfonyl, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkylsulfonyl, C 3 -C 8 -cycloalkylsulfonyl, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkenylsulfonyl, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkenylsulfonyl, di(C 1 -C 10 -alkyl)amino, C 1 -C 10 -alkylamino, C 2 -C 10 -alkenylamino, C 2 -C 10 -alkynylamino, C 1 -C 10 -alkyl-C 2 -C 10 -alkenylamino, C 1 -C 10 -alkyl-C 2 -C 10 -alkynylamino, C 1 -C 10 -haloalkylamino, C 2 -C 10 -haloalkenylamino, C 2 -C 10 -haloalkynylamino, C 3 -C 8 -cycloalkylamino, C 3 -C 8 -cycloalkenylamino, C 3 -C 8 -halocycloalkylamino, C 3 -C 8 -halocycloalkenylamino, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkylamino, C 4 -C 8 -cycloalkenyl-C 1 -C 4 -alkylamino, C 3 -C 8 -cycloalkyl-C 2 -C 4 -alkenylamino, C 4 -C 8 -cycloalkenyl-C 2 -C 4 -alkenylamino, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkylamino, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkylamino, C 1 -C 10 -alkynyl-C 3 -C 8 -cycloalkylamino, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkenylamino, C 1 -C 10 -alkenyl-C 3 -C 8 -cycloalkenylamino,
tri(C 1 -C 10 -alkyl)silyl, aryl, aryloxy, arylthio, arylamino, aryl-C 1 -C 4 -alkoxy, aryl-C 3 -C 4 -alkenyloxy, aryl-C 2 -C 4 -alkenylthio, aryl-C 1 -C 4 -alkylamino, aryl-C 3 -C 4 -alkenylamino, triarylsilyl, wherein aryl is phenyl, naphthyl or biphenyl, or
a saturated, partially unsaturated or unsaturated 3- to 8-membered ring system which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, wherein these aryl and these heterocyclic ringsystems are unsubstituted or substituted with any combination of from 1 to 6 groups selected from halogen, cyano, nitro, amino, hydroxy, mercapto, C 1 -C 4 -alkyl, C 3 -C 8 -cycloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, di(C 1 -C 4 -alkyl)amino, C 1 -C 4 -alkylamino, C 1 -C 4 -haloalkylamino, formyl and C 1 -C 4 -alkylcarbonyl;
Q 1 is hydrogen, halogen, cyano, C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl;
Q 2 is halogen, cyano, C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl;
Q 3 is halogen; or C 1 -C 10 -alkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkyl, C 1 -C 10 -haloalkyl-C 3 -C 8 -cycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C 1 -C 10 -haloalkoxy, C 1 -C 10 -alkylthio, C 1 -C 10 -haloalkylthio, C 1 -C 10 -alkylsulfinyl, C 1 -C 10 -haloalkylsulfinyl, C 1 -C 10 -alkylsulfonyl, C 1 -C 10 -haloalkylsulfonyl, and C 1 -C 10 -alkoxycarbonyl; or
Q 3 is OR 14 , S(O) q R 14 , NR 15 R 16 , OS(O) 2 R 17 , NR 16 S(O) 2 R 17 , C(S)NH 2 , C(R 18 )═NOR 18 , C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 10 -alkylaminothiocarbonyl, or di(C 1 -C 10 -alkyl)aminothiocarbonyl;
R 14 is C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -alkyl-C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl-C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl-C 3 -C 8 -cycloalkyl, or C 1 -C 10 -haloalkylcarbonyl, each unsubstituted or substituted with 1 R 19 ;
R 15 is C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 1 -C 4 -alkyl-C 3 -C 8 -cycloalkyl, C 1 -C 4 -haloalkyl-C 3 -C 8 -cycloalkyl, or C 1 -C 10 -haloalkylcarbonyl, each unsubstituted or substituted with 1 R 19 ;
R 16 is hydrogen; or C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 1 -C 4 -alkyl-C 3 -C 8 -cycloalkyl, or C 1 -C 4 -haloalkyl-C 3 -C 8 -cycloalkyl, each unsubstituted or substituted with 1 R 19 ;
R 17 is C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 1 -C 4 -alkyl-C 3 -C 8 -cycloalkyl, or C 1 -C 4 -haloalkyl-C 3 -C 8 -cycloalkyl, each unsubstituted or substituted with 1 R 19 ;
R 19 is cyano, nitro, C 1 -C 10 -alkoxy, C 1 -C 10 -haloalkoxy, C 1 -C 10 -haloalkylthio, C 1 -C 10 -alkylsulfinyl, C 1 -C 10 -haloalkylsulfinyl, C 1 -C 10 -alkylsulfonyl C 1 -C 10 -haloalkylsulfonyl, C 1 -C 10 -alkoxycarbonyl, C 1 -C 10 -alkylamino, or di(C 1 -C 10 -alkyl)amino; or
R 19 is phenyl or a heteroaromatic 5- or 6-membered ring which contains 1 to 4 heteroatoms selected from oxygen, nitrogen, sulfur, the phenyl radical and the heteroaromatic ring being unsubstituted or substituted with any combination of from 1 to 3 groups selected from halogen, cyano, nitro, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 3 -C 10 -haloalkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 1 -C 10 -alkoxy, C 1 -C 10 -haloalkoxy, C 1 -C 10 -alkylthio, C 1 -C 10 -alkylsulfinyl, C 1 -C 10 -alkylsulfonyl, C 1 -C 10 -alkylamino, di(C 1 -C 10 -alkyl)amino, C 3 -C 8 -cycloalkylamino, C 1 -C 10 -alkyl-C 3 -C 8 -cycloalkylamino, C 1 -C 10 -alkylcarbonyl, C 1 -C 10 -alkoxycarbonyl, C 1 -C 10 -alkylaminocarbonyl, di(C 1 -C 10 -alkyl)aminocarbonyl and tri(C 1 -C 10 )-alkylsilyl;
R 18 is the same or different: hydrogen, C 1 -C 10 -alkyl, or C 1 -C 10 -haloalkyl;
q is 0, 1 or 2;
Q 4 is halogen or C 1 -C 4 -haloalkyl
X and Y are each oxygen;
V and V′ are each CH;
W is N;
n is 0 or 1;
p is 1;
and/or an enantiomer, a salt, and/or an N-oxide thereof.
3 : The compound of claim 2 , wherein
Q 3 is halogen, C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkynyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, each unsubstituted or independently substituted with 1 to 2 groups selected from cyano, C 1 -C 10 -alkoxy, C 1 -C 10 -haloalkoxy or C 1 -C 10 -alkylthio, or Q 3 is OR 14 , S(O) q R 14 , NR 15 R 16 , OS(O) 2 R 17 , C(S)NH 2 , C(R 18 )═NOR 18 ; wherein
R 14 is C 1 -C 10 -alkyl or C 3 -C 8 -cycloalkyl unsubstituted or substituted with 1 R 19 ; and
R 15 is C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -alkynyl, each unsubstituted or substituted with 1 R 19 ; and
R 16 is hydrogen, C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -alkynyl, each unsubstituted or substituted with 1 R 19 ; and
R 17 is C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -alkynyl, C 3 -C 8 -cycloalkyl, each unsubstituted or substituted with 1 R 19 ; and
R 18 is hydrogen, C 1 -C 10 -alkyl, or C 1 -C 10 -haloalkyl; and
R 19 is cyano, nitro, C 1 -C 10 -alkoxy, C 1 -C 10 -haloalkoxy, C 1 -C 10 -alkylthio, C 1 -C 10 -haloalkylthio;
Q 4 is halogen and is in the ortho-position.
4 : The compound of claim 2 , wherein
Q 3 is halogen, C 1 -C 4 -haloalkyl or C 1 -C 4 -haloalkoxy.
5 : The compound of claim 2 , wherein
R 2 and R 3 each independently are C 1 -C 10 -alkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -alkynyl, C 3 -C 8 -cycloalkyl, or phenyl, wherein these groups are unsubstituted or substituted by any combination of 1 to 6 groups selected from R 11 ,
R 11 is halogen, cyano, nitro, hydroxy, mercapto, amino, C 1 -C 10 -alkoxy, C 1 -C 10 -haloalkoxy, C 3 -C 8 -cycloalkoxy, C 1 -C 10 -alkoxycarbonyl, C 1 -C 10 -aIkylcarbonyloxy, C 1 -C 10 -alkanamido, C 1 -C 10 -alkylthio, C 1 -C 10 -alkylsulfinyl, C 1 -C 10 -alkylsulfonyl, di(C 1 -C 10 -alkyl)amino or C 1 -C 10 -alkylamino.
6 : A compound of the formula IA
wherein
Q 1 denotes hydrogen, chlorine, bromine, fluorine or cyano;
Q 3 denotes CF 3 or bromine; and
A in each case corresponds to a row of the Table below,
TABLE C
No.
A
R e
R f
IA-139
CH 3
CH 3
IA-140
A 1 .1
CH 2 CH 3
CH 3
IA-141
A 1 .1
CH═CH 2
CH 3
IA-142
A 1 .1
CH 2 CH 2 CH 3
CH 3
IA-143
A 1 .1
CH(CH 3 ) 2
CH 3
IA-144
A 1 .1
CH 2 CH 2 CH 2 CH 3
CH 3
IA-145
A 1 .1
C(CH 3 ) 3
CH 3
IA-146
A 1 .1
CH 2 CH(CH 3 ) 2
CH 3
IA-147
A 1 .1
CH(CH 3 )CH 2 CH 3
CH 3
IA-148
A 1 .1
CH 2 CHCH 2
CH 3
IA-149
A 1 .1
CH 2 CCH
CH 3
IA-150
A 1 .1
CH(CH 3 )CH═CH 2
CH 3
IA-151
A 1 .1
CHF 2
CH 3
IA-152
A 1 .1
CH 2 Cl
CH 3
IA-153
A 1 .1
CH 2 CH 2 CN
CH 3
IA-154
A 1 .1
CH 2 CH 2 Cl
CH 3
IA-155
A 1 .1
CH 2 CH 2 OH
CH 3
IA-156
A 1 .1
CH 2 CH 2 CH 2 OH
CH 3
IA-157
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 3
IA-158
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 3
IA-159
A 1 .1
CH 2 SCH 3
CH 3
IA-160
A 1 .1
(CH 2 ) 3 SCH 3
CH 3
IA-161
A 1 .1
CH 2 S(═O)CH 3
CH 3
IA-162
A 1 .1
CH 2 S(═O) 2 CH 3
CH 3
IA-163
A 1 .1
CH 2 C(═O)CH 3
CH 3
IA-164
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 3
IA-165
A 1 .1
CH 2 COOH
CH 3
IA-166
A 1 .1
CH 2 COOCH 3
CH 3
IA-167
A 1 .1
CH 2 COOCH 2 CH 3
CH 3
IA-168
A 1 .1
cyclo-C 3 H 5
CH 3
IA-169
A 1 .1
cyclo-C 4 H 7
CH 3
IA-170
A 1 .1
cyclo-C 5 H 9
CH 3
IA-171
A 1 .1
cyclo-C 6 H 11
CH 3
IA-172
A 1 .1
C 6 H 5
CH 3
IA-173
A 1 .1
CH 2 CH 3
CH 2 CH 3
IA-174
A 1 .1
CH═CH 2
CH 2 CH 3
IA-175
A 1 .1
CH 2 CH 2 CH 3
CH 2 CH 3
IA-176
A 1 .1
CH(CH 3 ) 2
CH 2 CH 3
IA-177
A 1 .1
CH 2 CH 2 CH 2 CH 3
CH 2 CH 3
IA-178
A 1 .1
C(CH 3 ) 3
CH 2 CH 3
IA-179
A 1 .1
CH 2 CH(CH 3 ) 2
CH 2 CH 3
IA-180
A 1 .1
CH(CH 3 )CH 2 CH 3
CH 2 CH 3
IA-181
A 1 .1
CH 2 CHCH 2
CH 2 CH 3
IA-182
A 1 .1
CH 2 CCH
CH 2 CH 3
IA-183
A 1 .1
CH(CH 3 )CH═CH 2
CH 2 CH 3
IA-184
A 1 .1
CHF 2
CH 2 CH 3
IA-185
A 1 .1
CH 2 Cl
CH 2 CH 3
IA-186
A 1 .1
CH 2 CH 2 CN
CH 2 CH 3
IA-187
A 1 .1
CH 2 CH 2 Cl
CH 2 CH 3
IA-188
A 1 .1
CH 2 CH 2 OH
CH 2 CH 3
IA-189
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 3
IA-190
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 3
IA-191
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 3
IA-192
A 1 .1
CH 2 SCH 3
CH 2 CH 3
IA-193
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 3
IA-194
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 3
IA-195
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 3
IA-196
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 3
IA-197
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 3
IA-198
A 1 .1
CH 2 COOH
CH 2 CH 3
IA-199
A 1 .1
CH 2 COOCH 3
CH 2 CH 3
IA-200
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 3
IA-201
A 1 .1
cyclo-C 3 H 5
CH 2 CH 3
IA-202
A 1 .1
cyclo-C 4 H 7
CH 2 CH 3
IA-203
A 1 .1
cyclo-C 5 H 9
CH 2 CH 3
IA-204
A 1 .1
cyclo-C 6 H 11
CH 2 CH 3
IA-205
A 1 .1
C 6 H 5
CH 2 CH 3
IA-206
A 1 .1
CH═CH 2
CH═CH 2
IA-207
A 1 .1
CH 2 CH 2 CH 3
CH═CH 2
IA-208
A 1 .1
CH(CH 3 ) 2
CH═CH 2
IA-209
A 1 .1
CH 2 CH 2 CH 2 CH 3
CH═CH 2
IA-210
A 1 .1
C(CH 3 ) 3
CH═CH 2
IA-211
A 1 .1
CH 2 CH(CH 3 ) 2
CH═CH 2
IA-212
A 1 .1
CH(CH 3 )CH 2 CH 3
CH═CH 2
IA-213
A 1 .1
CH 2 CHCH 2
CH═CH 2
IA-214
A 1 .1
CH 2 CCH
CH═CH 2
IA-215
A 1 .1
CH(CH 3 )CH═CH 2
CH═CH 2
IA-216
A 1 .1
CHF 2
CH═CH 2
IA-217
A 1 .1
CH 2 Cl
CH═CH 2
IA-218
A 1 .1
CH 2 CH 2 CN
CH═CH 2
IA-219
A 1 .1
CH 2 CH 2 Cl
CH═CH 2
IA-220
A 1 .1
CH 2 CH 2 OH
CH═CH 2
IA-221
A 1 .1
CH 2 CH 2 CH 2 OH
CH═CH 2
IA-222
A 1 .1
CH 2 CH(OH)CH 2 OH
CH═CH 2
IA-223
A 1 .1
CH 2 CH(OCH 3 ) 2
CH═CH 2
IA-224
A 1 .1
CH 2 SCH 3
CH═CH 2
IA-225
A 1 .1
(CH 2 ) 3 SCH 3
CH═CH 2
IA-226
A 1 .1
CH 2 S(═O)CH 3
CH═CH 2
IA-227
A 1 .1
CH 2 S(═O) 2 CH 3
CH═CH 2
IA-228
A 1 .1
CH 2 C(═O)CH 3
CH═CH 2
IA-229
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH═CH 2
IA-230
A 1 .1
CH 2 COOH
CH═CH 2
IA-231
A 1 .1
CH 2 COOCH 3
CH═CH 2
IA-232
A 1 .1
CH 2 COOCH 2 CH 3
CH═CH 2
IA-233
A 1 .1
cyclo-C 3 H 5
CH═CH 2
IA-234
A 1 .1
cyclo-C 4 H 7
CH═CH 2
IA-235
A 1 .1
cyclo-C 5 H 9
CH═CH 2
IA-236
A 1 .1
cyclo-C 6 H 11
CH═CH 2
IA-237
A 1 .1
C 6 H 5
CH═CH 2
IA-238
A 1 .1
CH 2 CH 2 CH 3
CH 2 CH 2 CH 3
IA-239
A 1 .1
CH(CH 3 ) 2
CH 2 CH 2 CH 3
IA-240
A 1 .1
CH 2 CH 2 CH 2 CH 3
CH 2 CH 2 CH 3
IA-241
A 1 .1
C(CH 3 ) 3
CH 2 CH 2 CH 3
IA-242
A 1 .1
CH 2 CH(CH 3 ) 2
CH 2 CH 2 CH 3
IA-243
A 1 .1
CH(CH 3 )CH 2 CH 3
CH 2 CH 2 CH 3
IA-244
A 1 .1
CH 2 CHCH 2
CH 2 CH 2 CH 3
IA-245
A 1 .1
CH 2 CCH
CH 2 CH 2 CH 3
IA-246
A 1 .1
CH(CH 3 )CH═CH 2
CH 2 CH 2 CH 3
IA-247
A 1 .1
CHF 2
CH 2 CH 2 CH 3
IA-248
A 1 .1
CH 2 Cl
CH 2 CH 2 CH 3
IA-249
A 1 .1
CH 2 CH 2 CN
CH 2 CH 2 CH 3
IA-250
A 1 .1
CH 2 CH 2 Cl
CH 2 CH 2 CH 3
IA-251
A 1 .1
CH 2 CH 2 OH
CH 2 CH 2 CH 3
IA-252
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CH 3
IA-253
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CH 3
IA-254
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CH 3
IA-255
A 1 .1
CH 2 SCH 3
CH 2 CH 2 CH 3
IA-256
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 2 CH 3
IA-257
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 2 CH 3
IA-258
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CH 3
IA-259
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 2 CH 3
IA-260
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CH 3
IA-261
A 1 .1
CH 2 COOH
CH 2 CH 2 CH 3
IA-262
A 1 .1
CH 2 COOCH 3
CH 2 CH 2 CH 3
IA-263
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 2 CH 3
IA-264
A 1 .1
cyclo-C 3 H 5
CH 2 CH 2 CH 3
IA-265
A 1 .1
cyclo-C 4 H 7
CH 2 CH 2 CH 3
IA-266
A 1 .1
cyclo-C 5 H 9
CH 2 CH 2 CH 3
IA-267
A 1 .1
cyclo-C 6 H 11
CH 2 CH 2 CH 3
IA-268
A 1 .1
C 6 H 5
CH 2 CH 2 CH 3
IA-269
A 1 .1
CH(CH 3 ) 2
CH(CH 3 ) 2
IA-270
A 1 .1
CH 2 CH 2 CH 2 CH 3
CH(CH 3 ) 2
IA-271
A 1 .1
C(CH 3 ) 3
CH(CH 3 ) 2
IA-272
A 1 .1
CH 2 CH(CH 3 ) 2
CH(CH 3 ) 2
IA-273
A 1 .1
CH(CH 3 )CH 2 CH 3
CH(CH 3 ) 2
IA-274
A 1 .1
CH 2 CHCH 2
CH(CH 3 ) 2
IA-275
A 1 .1
CH 2 CCH
CH(CH 3 ) 2
IA-276
A 1 .1
CH(CH 3 )CH═CH 2
CH(CH 3 ) 2
IA-277
A 1 .1
CHF 2
CH(CH 3 ) 2
IA-278
A 1 .1
CH 2 Cl
CH(CH 3 ) 2
IA-279
A 1 .1
CH 2 CH 2 CN
CH(CH 3 ) 2
IA-280
A 1 .1
CH 2 CH 2 Cl
CH(CH 3 ) 2
IA-281
A 1 .1
CH 2 CH 2 OH
CH(CH 3 ) 2
IA-282
A 1 .1
CH 2 CH 2 CH 2 OH
CH(CH 3 ) 2
IA-283
A 1 .1
CH 2 CH(OH)CH 2 OH
CH(CH 3 ) 2
IA-284
A 1 .1
CH 2 CH(OCH 3 ) 2
CH(CH 3 ) 2
IA-285
A 1 .1
CH 2 SCH 3
CH(CH 3 ) 2
IA-286
A 1 .1
(CH 2 ) 3 SCH 3
CH(CH 3 ) 2
IA-287
A 1 .1
CH 2 S(═O)CH 3
CH(CH 3 ) 2
IA-288
A 1 .1
CH 2 S(═O) 2 CH 3
CH(CH 3 ) 2
IA-289
A 1 .1
CH 2 C(═O)CH 3
CH(CH 3 ) 2
IA-290
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH(CH 3 ) 2
IA-291
A 1 .1
CH 2 COOH
CH(CH 3 ) 2
IA-292
A 1 .1
CH 2 COOCH 3
CH(CH 3 ) 2
IA-293
A 1 .1
CH 2 COOCH 2 CH 3
CH(CH 3 ) 2
IA-294
A 1 .1
cyclo-C 3 H 5
CH(CH 3 ) 2
IA-295
A 1 .1
cyclo-C 4 H 7
CH(CH 3 ) 2
IA-296
A 1 .1
cyclo-C 5 H 9
CH(CH 3 ) 2
IA-297
A 1 .1
cyclo-C 6 H 11
CH(CH 3 ) 2
IA-298
A 1 .1
C 6 H 5
CH(CH 3 ) 2
IA-299
A 1 .1
CH 2 CH 2 CH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-300
A 1 .1
C(CH 3 ) 3
CH 2 CH 2 CH 2 CH 3
IA-301
A 1 .1
CH 2 CH(CH 3 ) 2
CH 2 CH 2 CH 2 CH 3
IA-302
A 1 .1
CH(CH 3 )CH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-303
A 1 .1
CH 2 CHCH 2
CH 2 CH 2 CH 2 CH 3
IA-304
A 1 .1
CH 2 CCH
CH 2 CH 2 CH 2 CH 3
IA-305
A 1 .1
CH(CH 3 )CH═CH 2
CH 2 CH 2 CH 2 CH 3
IA-306
A 1 .1
CHF 2
CH 2 CH 2 CH 2 CH 3
IA-307
A 1 .1
CH 2 Cl
CH 2 CH 2 CH 2 CH 3
IA-308
A 1 .1
CH 2 CH 2 CN
CH 2 CH 2 CH 2 CH 3
IA-309
A 1 .1
CH 2 CH 2 Cl
CH 2 CH 2 CH 2 CH 3
IA-310
A 1 .1
CH 2 CH 2 OH
CH 2 CH 2 CH 2 CH 3
IA-311
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CH 2 CH 3
IA-312
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CH 2 CH 3
IA-313
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CH 2 CH 3
IA-314
A 1 .1
CH 2 SCH 3
CH 2 CH 2 CH 2 CH 3
IA-315
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 2 CH 2 CH 3
IA-316
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 2 CH 2 CH 3
IA-317
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-318
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 2 CH 2 CH 3
IA-319
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-320
A 1 .1
CH 2 COOH
CH 2 CH 2 CH 2 CH 3
IA-321
A 1 .1
CH 2 COOCH 3
CH 2 CH 2 CH 2 CH 3
IA-322
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-323
A 1 .1
cyclo-C 3 H 5
CH 2 CH 2 CH 2 CH 3
IA-324
A 1 .1
cyclo-C 4 H 7
CH 2 CH 2 CH 2 CH 3
IA-325
A 1 .1
cyclo-C 5 H 9
CH 2 CH 2 CH 2 CH 3
IA-326
A 1 .1
cyclo-C 6 H 11
CH 2 CH 2 CH 2 CH 3
IA-327
A 1 .1
C 6 H 5
CH 2 CH 2 CH 2 CH 3
IA-328
A 1 .1
C(CH 3 ) 3
C(CH 3 ) 3
IA-329
A 1 .1
CH 2 CH(CH 3 ) 2
C(CH 3 ) 3
IA-330
A 1 .1
CH(CH 3 )CH 2 CH 3
C(CH 3 ) 3
IA-331
A 1 .1
CH 2 CHCH 2
C(CH 3 ) 3
IA-332
A 1 .1
CH 2 CCH
C(CH 3 ) 3
IA-333
A 1 .1
CH(CH 3 )CH═CH 2
C(CH 3 ) 3
IA-334
A 1 .1
CHF 2
C(CH 3 ) 3
IA-335
A 1 .1
CH 2 Cl
C(CH 3 ) 3
IA-336
A 1 .1
CH 2 CH 2 CN
C(CH 3 ) 3
IA-337
A 1 .1
CH 2 CH 2 Cl
C(CH 3 ) 3
IA-338
A 1 .1
CH 2 CH 2 OH
C(CH 3 ) 3
IA-339
A 1 .1
CH 2 CH 2 CH 2 OH
C(CH 3 ) 3
IA-340
A 1 .1
CH 2 CH(OH)CH 2 OH
C(CH 3 ) 3
IA-341
A 1 .1
CH 2 CH(OCH 3 ) 2
C(CH 3 ) 3
IA-342
A 1 .1
CH 2 SCH 3
C(CH 3 ) 3
IA-343
A 1 .1
(CH 2 ) 3 SCH 3
C(CH 3 ) 3
IA-344
A 1 .1
CH 2 S(═O)CH 3
C(CH 3 ) 3
IA-345
A 1 .1
CH 2 S(═O) 2 CH 3
C(CH 3 ) 3
IA-346
A 1 .1
CH 2 C(═O)CH 3
C(CH 3 ) 3
IA-347
A 1 .1
CH 2 C(═O)CH 2 CH 3
C(CH 3 ) 3
IA-348
A 1 .1
CH 2 COOH
C(CH 3 ) 3
IA-349
A 1 .1
CH 2 COOCH 3
C(CH 3 ) 3
IA-350
A 1 .1
CH 2 COOCH 2 CH 3
C(CH 3 ) 3
IA-351
A 1 .1
cyclo-C 3 H 5
C(CH 3 ) 3
IA-352
A 1 .1
cyclo-C 4 H 7
C(CH 3 ) 3
IA-353
A 1 .1
cyclo-C 5 H 9
C(CH 3 ) 3
IA-354
A 1 .1
cyclo-C 6 H 11
C(CH 3 ) 3
IA-355
A 1 .1
C 6 H 5
C(CH 3 ) 3
IA-356
A 1 .1
CH 2 CH(CH 3 ) 2
CH 2 CH(CH 3 ) 2
IA-357
A 1 .1
CH(CH 3 )CH 2 CH 3
CH 2 CH(CH 3 ) 2
IA-358
A 1 .1
CH 2 CHCH 2
CH 2 CH(CH 3 ) 2
IA-359
A 1 .1
CH 2 CCH
CH 2 CH(CH 3 ) 2
IA-360
A 1 .1
CH(CH 3 )CH═CH 2
CH 2 CH(CH 3 ) 2
IA-361
A 1 .1
CHF 2
CH 2 CH(CH 3 ) 2
IA-362
A 1 .1
CH 2 Cl
CH 2 CH(CH 3 ) 2
IA-363
A 1 .1
CH 2 CH 2 CN
CH 2 CH(CH 3 ) 2
IA-364
A 1 .1
CH 2 CH 2 Cl
CH 2 CH(CH 3 ) 2
IA-365
A 1 .1
CH 2 CH 2 OH
CH 2 CH(CH 3 ) 2
IA-366
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH(CH 3 ) 2
IA-367
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH(CH 3 ) 2
IA-368
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH(CH 3 ) 2
IA-369
A 1 .1
CH 2 SCH 3
CH 2 CH(CH 3 ) 2
IA-370
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH(CH 3 ) 2
IA-371
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH(CH 3 ) 2
IA-372
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH(CH 3 ) 2
IA-373
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH(CH 3 ) 2
IA-374
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH(CH 3 ) 2
IA-375
A 1 .1
CH 2 COOH
CH 2 CH(CH 3 ) 2
IA-376
A 1 .1
CH 2 COOCH 3
CH 2 CH(CH 3 ) 2
IA-377
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH(CH 3 ) 2
IA-378
A 1 .1
cyclo-C 3 H 5
CH 2 CH(CH 3 ) 2
IA-379
A 1 .1
cyclo-C 4 H 7
CH 2 CH(CH 3 ) 2
IA-380
A 1 .1
cyclo-C 5 H 9
CH 2 CH(CH 3 ) 2
IA-381
A 1 .1
cyclo-C 6 H 11
CH 2 CH(CH 3 ) 2
IA-382
A 1 .1
C 6 H 5
CH 2 CH(CH 3 ) 2
IA-383
A 1 .1
CH(CH 3 )CH 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-384
A 1 .1
CH 2 CHCH 2
CH(CH 3 )CH 2 CH 3
IA-385
A 1 .1
CH 2 CCH
CH(CH 3 )CH 2 CH 3
IA-386
A 1 .1
CH(CH 3 )CH═CH 2
CH(CH 3 )CH 2 CH 3
IA-387
A 1 .1
CHF 2
CH(CH 3 )CH 2 CH 3
IA-388
A 1 .1
CH 2 Cl
CH(CH 3 )CH 2 CH 3
IA-389
A 1 .1
CH 2 CH 2 CN
CH(CH 3 )CH 2 CH 3
IA-390
A 1 .1
CH 2 CH 2 Cl
CH(CH 3 )CH 2 CH 3
IA-391
A 1 .1
CH 2 CH 2 OH
CH(CH 3 )CH 2 CH 3
IA-392
A 1 .1
CH 2 CH 2 CH 2 OH
CH(CH 3 )CH 2 CH 3
IA-393
A 1 .1
CH 2 CH(OH)CH 2 OH
CH(CH 3 )CH 2 CH 3
IA-394
A 1 .1
CH 2 CH(OCH 3 ) 2
CH(CH 3 )CH 2 CH 3
IA-395
A 1 .1
CH 2 SCH 3
CH(CH 3 )CH 2 CH 3
IA-396
A 1 .1
(CH 2 ) 3 SCH 3
CH(CH 3 )CH 2 CH 3
IA-397
A 1 .1
CH 2 S(═O)CH 3
CH(CH 3 )CH 2 CH 3
IA-398
A 1 .1
CH 2 S(═O) 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-399
A 1 .1
CH 2 C(═O)CH 3
CH(CH 3 )CH 2 CH 3
IA-400
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-401
A 1 .1
CH 2 COOH
CH(CH 3 )CH 2 CH 3
IA-402
A 1 .1
CH 2 COOCH 3
CH(CH 3 )CH 2 CH 3
IA-403
A 1 .1
CH 2 COOCH 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-404
A 1 .1
cyclo-C 3 H 5
CH(CH 3 )CH 2 CH 3
IA-405
A 1 .1
cyclo-C 4 H 7
CH(CH 3 )CH 2 CH 3
IA-406
A 1 .1
cyclo-C 5 H 9
CH(CH 3 )CH 2 CH 3
IA-407
A 1 .1
cyclo-C 6 H 11
CH(CH 3 )CH 2 CH 3
IA-408
A 1 .1
C 6 H 5
CH(CH 3 )CH 2 CH 3
IA-409
A 1 .1
CH 2 CHCH 2
CH 2 CHCH 2
IA-410
A 1 .1
CH 2 CCH
CH 2 CHCH 2
IA-411
A 1 .1
CH(CH 3 )CH═CH 2
CH 2 CHCH 2
IA-412
A 1 .1
CHF 2
CH 2 CHCH 2
IA-413
A 1 .1
CH 2 Cl
CH 2 CHCH 2
IA-414
A 1 .1
CH 2 CH 2 CN
CH 2 CHCH 2
IA-415
A 1 .1
CH 2 CH 2 Cl
CH 2 CHCH 2
IA-416
A 1 .1
CH 2 CH 2 OH
CH 2 CHCH 2
IA-417
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CHCH 2
IA-418
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CHCH 2
IA-419
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CHCH 2
IA-420
A 1 .1
CH 2 SCH 3
CH 2 CHCH 2
IA-421
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CHCH 2
IA-422
A 1 .1
CH 2 S(═O)CH 3
CH 2 CHCH 2
IA-423
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CHCH 2
IA-424
A 1 .1
CH 2 C(═O)CH 3
CH 2 CHCH 2
IA-425
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CHCH 2
IA-426
A 1 .1
CH 2 COOH
CH 2 CHCH 2
IA-427
A 1 .1
CH 2 COOCH 3
CH 2 CHCH 2
IA-428
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CHCH 2
IA-429
A 1 .1
cyclo-C 3 H 5
CH 2 CHCH 2
IA-430
A 1 .1
cyclo-C 4 H 7
CH 2 CHCH 2
IA-431
A 1 .1
cyclo-C 5 H 9
CH 2 CHCH 2
IA-432
A 1 .1
cyclo-C 6 H 11
CH 2 CHCH 2
IA-433
A 1 .1
C 6 H 5
CH 2 CHCH 2
IA-434
A 1 .1
CH 2 CCH
CH 2 CCH
IA-435
A 1 .1
CH(CH 3 )CH═CH 2
CH 2 CCH
IA-436
A 1 .1
CHF 2
CH 2 CCH
IA-437
A 1 .1
CH 2 Cl
CH 2 CCH
IA-438
A 1 .1
CH 2 CH 2 CN
CH 2 CCH
IA-439
A 1 .1
CH 2 CH 2 Cl
CH 2 CCH
IA-440
A 1 .1
CH 2 CH 2 OH
CH 2 CCH
IA-441
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CCH
IA-442
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CCH
IA-443
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CCH
IA-444
A 1 .1
CH 2 SCH 3
CH 2 CCH
IA-445
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CCH
IA-446
A 1 .1
CH 2 S(═O)CH 3
CH 2 CCH
IA-447
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CCH
IA-448
A 1 .1
CH 2 C(═O)CH 3
CH 2 CCH
IA-449
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CCH
IA-450
A 1 .1
CH 2 COOH
CH 2 CCH
IA-451
A 1 .1
CH 2 COOCH 3
CH 2 CCH
IA-452
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CCH
IA-453
A 1 .1
cyclo-C 3 H 5
CH 2 CCH
IA-454
A 1 .1
cyclo-C 4 H 7
CH 2 CCH
IA-455
A 1 .1
cyclo-C 5 H 9
CH 2 CCH
IA-456
A 1 .1
cyclo-C 6 H 11
CH 2 CCH
IA-457
A 1 .1
C 6 H 5
CH 2 CCH
IA-458
A 1 .1
CH(CH 3 )CH═CH 2
CH(CH 3 )CH═CH 2
IA-459
A 1 .1
CHF 2
CH(CH 3 )CH═CH 2
IA-460
A 1 .1
CH 2 Cl
CH(CH 3 )CH═CH 2
IA-461
A 1 .1
CH 2 CH 2 CN
CH(CH 3 )CH═CH 2
IA-462
A 1 .1
CH 2 CH 2 Cl
CH(CH 3 )CH═CH 2
IA-463
A 1 .1
CH 2 CH 2 OH
CH(CH 3 )CH═CH 2
IA-464
A 1 .1
CH 2 CH 2 CH 2 OH
CH(CH 3 )CH═CH 2
IA-465
A 1 .1
CH 2 CH(OH)CH 2 OH
CH(CH 3 )CH═CH 2
IA-466
A 1 .1
CH 2 CH(OCH 3 ) 2
CH(CH 3 )CH═CH 2
IA-467
A 1 .1
CH 2 SCH 3
CH(CH 3 )CH═CH 2
IA-468
A 1 .1
(CH 2 ) 3 SCH 3
CH(CH 3 )CH═CH 2
IA-469
A 1 .1
CH 2 S(═O)CH 3
CH(CH 3 )CH═CH 2
IA-470
A 1 .1
CH 2 S(═O) 2 CH 3
CH(CH 3 )CH═CH 2
IA-471
A 1 .1
CH 2 C(═O)CH 3
CH(CH 3 )CH═CH 2
IA-472
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH(CH 3 )CH═CH 2
IA-473
A 1 .1
CH 2 COOH
CH(CH 3 )CH═CH 2
IA-474
A 1 .1
CH 2 COOCH 3
CH(CH 3 )CH═CH 2
IA-475
A 1 .1
CH 2 COOCH 2 CH 3
CH(CH 3 )CH═CH 2
IA-476
A 1 .1
cyclo-C 3 H 5
CH(CH 3 )CH═CH 2
IA-477
A 1 .1
cyclo-C 4 H 7
CH(CH 3 )CH═CH 2
IA-478
A 1 .1
cyclo-C 5 H 9
CH(CH 3 )CH═CH 2
IA-479
A 1 .1
cyclo-C 6 H 11
CH(CH 3 )CH═CH 2
IA-480
A 1 .1
C 6 H 5
CH(CH 3 )CH═CH 2
IA-481
A 1 .1
CHF 2
CHF 2
IA-482
A 1 .1
CH 2 Cl
CHF 2
IA-483
A 1 .1
CH 2 CH 2 CN
CHF 2
IA-484
A 1 .1
CH 2 CH 2 Cl
CHF 2
IA-485
A 1 .1
CH 2 CH 2 OH
CHF 2
IA-486
A 1 .1
CH 2 CH 2 CH 2 OH
CHF 2
IA-487
A 1 .1
CH 2 CH(OH)CH 2 OH
CHF 2
IA-488
A 1 .1
CH 2 CH(OCH 3 ) 2
CHF 2
IA-489
A 1 .1
CH 2 SCH 3
CHF 2
IA-490
A 1 .1
(CH 2 ) 3 SCH 3
CHF 2
IA-491
A 1 .1
CH 2 S(═O)CH 3
CHF 2
IA-492
A 1 .1
CH 2 S(═O) 2 CH 3
CHF 2
IA-493
A 1 .1
CH 2 C(═O)CH 3
CHF 2
IA-494
A 1 .1
CH 2 C(═O)CH 2 CH 3
CHF 2
IA-495
A 1 .1
CH 2 COOH
CHF 2
IA-496
A 1 .1
CH 2 COOCH 3
CHF 2
IA-497
A 1 .1
CH 2 COOCH 2 CH 3
CHF 2
IA-498
A 1 .1
cyclo-C 3 H 5
CHF 2
IA-499
A 1 .1
cyclo-C 4 H 7
CHF 2
IA-500
A 1 .1
cyclo-C 5 H 9
CHF 2
IA-501
A 1 .1
cyclo-C 6 H 11
CHF 2
IA-502
A 1 .1
C 6 H 5
CHF 2
IA-503
A 1 .1
CH 2 Cl
CH 2 Cl
IA-504
A 1 .1
CH 2 CH 2 CN
CH 2 Cl
IA-505
A 1 .1
CH 2 CH 2 Cl
CH 2 Cl
IA-506
A 1 .1
CH 2 CH 2 OH
CH 2 Cl
IA-507
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 Cl
IA-508
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 Cl
IA-509
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 Cl
IA-510
A 1 .1
CH 2 SCH 3
CH 2 Cl
IA-511
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 Cl
IA-512
A 1 .1
CH 2 S(═O)CH 3
CH 2 Cl
IA-513
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 Cl
IA-514
A 1 .1
CH 2 C(═O)CH 3
CH 2 Cl
IA-515
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 Cl
IA-516
A 1 .1
CH 2 COOH
CH 2 Cl
IA-517
A 1 .1
CH 2 COOCH 3
CH 2 Cl
IA-518
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 Cl
IA-519
A 1 .1
cyclo-C 3 H 5
CH 2 Cl
IA-520
A 1 .1
cyclo-C 4 H 7
CH 2 Cl
IA-521
A 1 .1
cyclo-C 5 H 9
CH 2 Cl
IA-522
A 1 .1
cyclo-C 6 H 11
CH 2 Cl
IA-523
A 1 .1
C 6 H 5
CH 2 Cl
IA-524
A 1 .1
CH 2 CH 2 CN
CH 2 CH 2 CN
IA-525
A 1 .1
CH 2 CH 2 Cl
CH 2 CH 2 CN
IA-526
A 1 .1
CH 2 CH 2 OH
CH 2 CH 2 CN
IA-527
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CN
IA-528
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CN
IA-529
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CN
IA-530
A 1 .1
CH 2 SCH 3
CH 2 CH 2 CN
IA-531
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 2 CN
IA-532
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 2 CN
IA-533
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CN
IA-534
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 2 CN
IA-535
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CN
IA-536
A 1 .1
CH 2 COOH
CH 2 CH 2 CN
IA-537
A 1 .1
CH 2 COOCH 3
CH 2 CH 2 CN
IA-538
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 2 CN
IA-539
A 1 .1
cyclo-C 3 H 5
CH 2 CH 2 CN
IA-540
A 1 .1
cyclo-C 4 H 7
CH 2 CH 2 CN
IA-541
A 1 .1
cyclo-C 5 H 9
CH 2 CH 2 CN
IA-542
A 1 .1
cyclo-C 6 H 11
CH 2 CH 2 CN
IA-543
A 1 .1
C 6 H 5
CH 2 CH 2 CN
IA-544
A 1 .1
CH 2 CH 2 Cl
CH 2 CH 2 Cl
IA-545
A 1 .1
CH 2 CH 2 OH
CH 2 CH 2 Cl
IA-546
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 2 Cl
IA-547
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 Cl
IA-548
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 Cl
IA-549
A 1 .1
CH 2 SCH 3
CH 2 CH 2 Cl
IA-550
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 2 Cl
IA-551
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 2 Cl
IA-552
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 2 Cl
IA-553
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 2 Cl
IA-554
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 Cl
IA-555
A 1 .1
CH 2 COOH
CH 2 CH 2 Cl
IA-556
A 1 .1
CH 2 COOCH 3
CH 2 CH 2 Cl
IA-557
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 2 Cl
IA-558
A 1 .1
cyclo-C 3 H 5
CH 2 CH 2 Cl
IA-559
A 1 .1
cyclo-C 4 H 7
CH 2 CH 2 Cl
IA-560
A 1 .1
cyclo-C 5 H 9
CH 2 CH 2 Cl
IA-561
A 1 .1
cyclo-C 6 H 11
CH 2 CH 2 Cl
IA-562
A 1 .1
C 6 H 5
CH 2 CH 2 Cl
IA-563
A 1 .1
CH 2 CH 2 OH
CH 2 CH 2 OH
IA-564
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 2 OH
IA-565
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 OH
IA-566
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 OH
IA-567
A 1 .1
CH 2 SCH 3
CH 2 CH 2 OH
IA-568
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 2 OH
IA-569
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 2 OH
IA-570
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 2 OH
IA-571
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 2 OH
IA-572
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 OH
IA-573
A 1 .1
CH 2 COOH
CH 2 CH 2 OH
IA-574
A 1 .1
CH 2 COOCH 3
CH 2 CH 2 OH
IA-575
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 2 OH
IA-576
A 1 .1
cyclo-C 3 H 5
CH 2 CH 2 OH
IA-577
A 1 .1
cyclo-C 4 H 7
CH 2 CH 2 OH
IA-578
A 1 .1
cyclo-C 5 H 9
CH 2 CH 2 OH
IA-579
A 1 .1
cyclo-C 6 H 11
CH 2 CH 2 OH
IA-580
A 1 .1
C 6 H 5
CH 2 CH 2 OH
IA-581
A 1 .1
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CH 2 OH
IA-582
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CH 2 OH
IA-583
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CH 2 OH
IA-584
A 1 .1
CH 2 SCH 3
CH 2 CH 2 CH 2 OH
IA-585
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH 2 CH 2 OH
IA-586
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH 2 CH 2 OH
IA-587
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CH 2 OH
IA-588
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH 2 CH 2 OH
IA-589
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CH 2 OH
IA-590
A 1 .1
CH 2 COOH
CH 2 CH 2 CH 2 OH
IA-591
A 1 .1
CH 2 COOCH 3
CH 2 CH 2 CH 2 OH
IA-592
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH 2 CH 2 OH
IA-593
A 1 .1
cyclo-C 3 H 5
CH 2 CH 2 CH 2 OH
IA-594
A 1 .1
cyclo-C 4 H 7
CH 2 CH 2 CH 2 OH
IA-595
A 1 .1
cyclo-C 5 H 9
CH 2 CH 2 CH 2 OH
IA-596
A 1 .1
cyclo-C 6 H 11
CH 2 CH 2 CH 2 OH
IA-597
A 1 .1
C 6 H 5
CH 2 CH 2 CH 2 OH
IA-598
A 1 .1
CH 2 CH(OH)CH 2 OH
CH 2 CH(OH)CH 2 OH
IA-599
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH(OH)CH 2 OH
IA-600
A 1 .1
CH 2 SCH 3
CH 2 CH(OH)CH 2 OH
IA-601
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH(OH)CH 2 OH
IA-602
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH(OH)CH 2 OH
IA-603
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH(OH)CH 2 OH
IA-604
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH(OH)CH 2 OH
IA-605
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH(OH)CH 2 OH
IA-606
A 1 .1
CH 2 COOH
CH 2 CH(OH)CH 2 OH
IA-607
A 1 .1
CH 2 COOCH 3
CH 2 CH(OH)CH 2 OH
IA-608
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH(OH)CH 2 OH
IA-609
A 1 .1
cyclo-C 3 H 5
CH 2 CH(OH)CH 2 OH
IA-610
A 1 .1
cyclo-C 4 H 7
CH 2 CH(OH)CH 2 OH
IA-611
A 1 .1
cyclo-C 5 H 9
CH 2 CH(OH)CH 2 OH
IA-612
A 1 .1
cyclo-C 6 H 11
CH 2 CH(OH)CH 2 OH
IA-613
A 1 .1
C 6 H 5
CH 2 CH(OH)CH 2 OH
IA-614
A 1 .1
CH 2 CH(OCH 3 ) 2
CH 2 CH(OCH 3 ) 2
IA-615
A 1 .1
CH 2 SCH 3
CH 2 CH(OCH 3 ) 2
IA-616
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 CH(OCH 3 ) 2
IA-617
A 1 .1
CH 2 S(═O)CH 3
CH 2 CH(OCH 3 ) 2
IA-618
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 CH(OCH 3 ) 2
IA-619
A 1 .1
CH 2 C(═O)CH 3
CH 2 CH(OCH 3 ) 2
IA-620
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 CH(OCH 3 ) 2
IA-621
A 1 .1
CH 2 COOH
CH 2 CH(OCH 3 ) 2
IA-622
A 1 .1
CH 2 COOCH 3
CH 2 CH(OCH 3 ) 2
IA-623
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 CH(OCH 3 ) 2
IA-624
A 1 .1
cyclo-C 3 H 5
CH 2 CH(OCH 3 ) 2
IA-625
A 1 .1
cyclo-C 4 H 7
CH 2 CH(OCH 3 ) 2
IA-626
A 1 .1
cyclo-C 5 H 9
CH 2 CH(OCH 3 ) 2
IA-627
A 1 .1
cyclo-C 6 H 11
CH 2 CH(OCH 3 ) 2
IA-628
A 1 .1
C 6 H 5
CH 2 CH(OCH 3 ) 2
IA-629
A 1 .1
CH 2 SCH 3
CH 2 SCH 3
IA-630
A 1 .1
(CH 2 ) 3 SCH 3
CH 2 SCH 3
IA-631
A 1 .1
CH 2 S(═O)CH 3
CH 2 SCH 3
IA-632
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 SCH 3
IA-633
A 1 .1
CH 2 C(═O)CH 3
CH 2 SCH 3
IA-634
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 SCH 3
IA-635
A 1 .1
CH 2 COOH
CH 2 SCH 3
IA-636
A 1 .1
CH 2 COOCH 3
CH 2 SCH 3
IA-637
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 SCH 3
IA-638
A 1 .1
cyclo-C 3 H 5
CH 2 SCH 3
IA-639
A 1 .1
cyclo-C 4 H 7
CH 2 SCH 3
IA-640
A 1 .1
cyclo-C 5 H 9
CH 2 SCH 3
IA-641
A 1 .1
cyclo-C 6 H 11
CH 2 SCH 3
IA-642
A 1 .1
C 6 H 5
CH 2 SCH 3
IA-643
A 1 .1
(CH 2 ) 3 SCH 3
(CH 2 ) 3 SCH 3
IA-644
A 1 .1
CH 2 S(═O)CH 3
(CH 2 ) 3 SCH 3
IA-645
A 1 .1
CH 2 S(═O) 2 CH 3
(CH 2 ) 3 SCH 3
IA-646
A 1 .1
CH 2 C(═O)CH 3
(CH 2 ) 3 SCH 3
IA-647
A 1 .1
CH 2 C(═O)CH 2 CH 3
(CH 2 ) 3 SCH 3
IA-648
A 1 .1
CH 2 COOH
(CH 2 ) 3 SCH 3
IA-649
A 1 .1
CH 2 COOCH 3
(CH 2 ) 3 SCH 3
IA-650
A 1 .1
CH 2 COOCH 2 CH 3
(CH 2 ) 3 SCH 3
IA-651
A 1 .1
cyclo-C 3 H 5
(CH 2 ) 3 SCH 3
IA-652
A 1 .1
cyclo-C 4 H 7
(CH 2 ) 3 SCH 3
IA-653
A 1 .1
cyclo-C 5 H 9
(CH 2 ) 3 SCH 3
IA-654
A 1 .1
cyclo-C 6 H 11
(CH 2 ) 3 SCH 3
IA-655
A 1 .1
C 6 H 5
(CH 2 ) 3 SCH 3
IA-656
A 1 .1
CH 2 S(═O)CH 3
CH 2 S(═O)CH 3
IA-657
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 S(═O)CH 3
IA-658
A 1 .1
CH 2 C(═O)CH 3
CH 2 S(═O)CH 3
IA-659
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 S(═O)CH 3
IA-660
A 1 .1
CH 2 COOH
CH 2 S(═O)CH 3
IA-661
A 1 .1
CH 2 COOCH 3
CH 2 S(═O)CH 3
IA-662
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 S(═O)CH 3
IA-663
A 1 .1
cyclo-C 3 H 5
CH 2 S(═O)CH 3
IA-664
A 1 .1
cyclo-C 4 H 7
CH 2 S(═O)CH 3
IA-665
A 1 .1
cyclo-C 5 H 9
CH 2 S(═O)CH 3
IA-666
A 1 .1
cyclo-C 6 H 11
CH 2 S(═O)CH 3
IA-667
A 1 .1
C 6 H 5
CH 2 S(═O)CH 3
IA-668
A 1 .1
CH 2 S(═O) 2 CH 3
CH 2 S(═O) 2 CH 3
IA-669
A 1 .1
CH 2 C(═O)CH 3
CH 2 S(═O) 2 CH 3
IA-670
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 S(═O) 2 CH 3
IA-671
A 1 .1
CH 2 COOH
CH 2 S(═O) 2 CH 3
IA-672
A 1 .1
CH 2 COOCH 3
CH 2 S(═O) 2 CH 3
IA-673
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 S(═O) 2 CH 3
IA-674
A 1 .1
cyclo-C 3 H 5
CH 2 S(═O) 2 CH 3
IA-675
A 1 .1
cyclo-C 4 H 7
CH 2 S(═O) 2 CH 3
IA-676
A 1 .1
cyclo-C 5 H 9
CH 2 S(═O) 2 CH 3
IA-677
A 1 .1
cyclo-C 6 H 11
CH 2 S(═O) 2 CH 3
IA-678
A 1 .1
C 6 H 5
CH 2 S(═O) 2 CH 3
IA-679
A 1 .1
CH 2 C(═O)CH 3
CH 2 C(═O)CH 3
IA-680
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 C(═O)CH 3
IA-681
A 1 .1
CH 2 COOH
CH 2 C(═O)CH 3
IA-682
A 1 .1
CH 2 COOCH 3
CH 2 C(═O)CH 3
IA-683
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 C(═O)CH 3
IA-684
A 1 .1
cyclo-C 3 H 5
CH 2 C(═O)CH 3
IA-685
A 1 .1
cyclo-C 4 H 7
CH 2 C(═O)CH 3
IA-686
A 1 .1
cyclo-C 5 H 9
CH 2 C(═O)CH 3
IA-687
A 1 .1
cyclo-C 6 H 11
CH 2 C(═O)CH 3
IA-688
A 1 .1
C 6 H 5
CH 2 C(═O)CH 3
IA-689
A 1 .1
CH 2 C(═O)CH 2 CH 3
CH 2 C(═O)CH 2 CH 3
IA-690
A 1 .1
CH 2 COOH
CH 2 C(═O)CH 2 CH 3
IA-691
A 1 .1
CH 2 COOCH 3
CH 2 C(═O)CH 2 CH 3
IA-692
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 C(═O)CH 2 CH 3
IA-693
A 1 .1
cyclo-C 3 H 5
CH 2 C(═O)CH 2 CH 3
IA-694
A 1 .1
cyclo-C 4 H 7
CH 2 C(═O)CH 2 CH 3
IA-695
A 1 .1
cyclo-C 5 H 9
CH 2 C(═O)CH 2 CH 3
IA-696
A 1 .1
cyclo-C 6 H 11
CH 2 C(═O)CH 2 CH 3
IA-697
A 1 .1
C 6 H 5
CH 2 C(═O)CH 2 CH 3
IA-698
A 1 .1
CH 2 COOH
CH 2 COOH
IA-699
A 1 .1
CH 2 COOCH 3
CH 2 COOH
IA-700
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 COOH
IA-701
A 1 .1
cyclo-C 3 H 5
CH 2 COOH
IA-702
A 1 .1
cyclo-C 4 H 7
CH 2 COOH
IA-703
A 1 .1
cyclo-C 5 H 9
CH 2 COOH
IA-704
A 1 .1
cyclo-C 6 H 11
CH 2 COOH
IA-705
A 1 .1
C 6 H 5
CH 2 COOH
IA-706
A 1 .1
CH 2 COOCH 3
CH 2 COOCH 3
IA-707
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 COOCH 3
IA-708
A 1 .1
cyclo-C 3 H 5
CH 2 COOCH 3
IA-709
A 1 .1
cyclo-C 4 H 7
CH 2 COOCH 3
IA-710
A 1 .1
cyclo-C 5 H 9
CH 2 COOCH 3
IA-711
A 1 .1
cyclo-C 6 H 11
CH 2 COOCH 3
IA-712
A 1 .1
C 6 H 5
CH 2 COOCH 3
IA-713
A 1 .1
CH 2 COOCH 2 CH 3
CH 2 COOCH 2 CH 3
IA-714
A 1 .1
cyclo-C 3 H 5
CH 2 COOCH 2 CH 3
IA-715
A 1 .1
cyclo-C 4 H 7
CH 2 COOCH 2 CH 3
IA-716
A 1 .1
cyclo-C 5 H 9
CH 2 COOCH 2 CH 3
IA-717
A 1 .1
cyclo-C 6 H 11
CH 2 COOCH 2 CH 3
IA-718
A 1 .1
C 6 H 5
CH 2 COOCH 2 CH 3
IA-719
A 1 .1
cyclo-C 3 H 5
cyclo-C 3 H 5
IA-720
A 1 .1
cyclo-C 4 H 7
cyclo-C 3 H 5
IA-721
A 1 .1
cyclo-C 5 H 9
cyclo-C 3 H 5
IA-722
A 1 .1
cyclo-C 6 H 11
cyclo-C 3 H 5
IA-723
A 1 .1
C 6 H 5
cyclo-C 3 H 5
IA-724
A 1 .1
cyclo-C 4 H 7
cyclo-C 4 H 7
IA-725
A 1 .1
cyclo-C 5 H 9
cyclo-C 4 H 7
IA-726
A 1 .1
cyclo-C 6 H 11
cyclo-C 4 H 7
IA-727
A 1 .1
C 6 H 5
cyclo-C 4 H 7
IA-728
A 1 .1
cyclo-C 5 H 9
cyclo-C 5 H 9
IA-729
A 1 .1
cyclo-C 6 H 11
cyclo-C 5 H 9
IA-730
A 1 .1
C 6 H 5
cyclo-C 5 H 9
IA-731
A 1 .1
cyclo-C 6 H 11
cyclo-C 6 H 11
IA-732
A 1 .1
C 6 H 5
cyclo-C 6 H 11
IA-733
A 1 .1
C 6 H 5
C 6 H 5
IA-734
CH 3
CH 3
IA-735
A 1 .2
CH 2 CH 3
CH 3
IA-736
A 1 .2
CH═CH 2
CH 3
IA-737
A 1 .2
CH 2 CH 2 CH 3
CH 3
IA-738
A 1 .2
CH(CH 3 ) 2
CH 3
IA-739
A 1 .2
CH 2 CH 2 CH 2 CH 3
CH 3
IA-740
A 1 .2
C(CH 3 ) 3
CH 3
IA-741
A 1 .2
CH 2 CH(CH 3 ) 2
CH 3
IA-742
A 1 .2
CH(CH 3 )CH 2 CH 3
CH 3
IA-743
A 1 .2
CH 2 CHCH 2
CH 3
IA-744
A 1 .2
CH 2 CCH
CH 3
IA-745
A 1 .2
CH(CH 3 )CH═CH 2
CH 3
IA-746
A 1 .2
CHF 2
CH 3
IA-747
A 1 .2
CH 2 Cl
CH 3
IA-748
A 1 .2
CH 2 CH 2 CN
CH 3
IA-749
A 1 .2
CH 2 CH 2 Cl
CH 3
IA-750
A 1 .2
CH 2 CH 2 OH
CH 3
IA-751
A 1 .2
CH 2 CH 2 CH 2 OH
CH 3
IA-752
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 3
IA-753
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 3
IA-754
A 1 .2
CH 2 SCH 3
CH 3
IA-755
A 1 .2
(CH 2 ) 3 SCH 3
CH 3
IA-756
A 1 .2
CH 2 S(═O)CH 3
CH 3
IA-757
A 1 .2
CH 2 S(═O) 2 CH 3
CH 3
IA-758
A 1 .2
CH 2 C(═O)CH 3
CH 3
IA-759
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 3
IA-760
A 1 .2
CH 2 COOH
CH 3
IA-761
A 1 .2
CH 2 COOCH 3
CH 3
IA-762
A 1 .2
CH 2 COOCH 2 CH 3
CH 3
IA-763
A 1 .2
cyclo-C 3 H 5
CH 3
IA-764
A 1 .2
cyclo-C 4 H 7
CH 3
IA-765
A 1 .2
cyclo-C 5 H 9
CH 3
IA-766
A 1 .2
cyclo-C 6 H 11
CH 3
IA-767
A 1 .2
C 6 H 5
CH 3
IA-768
A 1 .2
CH 2 CH 3
CH 2 CH 3
IA-769
A 1 .2
CH═CH 2
CH 2 CH 3
IA-770
A 1 .2
CH 2 CH 2 CH 3
CH 2 CH 3
IA-771
A 1 .2
CH(CH 3 ) 2
CH 2 CH 3
IA-772
A 1 .2
CH 2 CH 2 CH 2 CH 3
CH 2 CH 3
IA-773
A 1 .2
C(CH 3 ) 3
CH 2 CH 3
IA-774
A 1 .2
CH 2 CH(CH 3 ) 2
CH 2 CH 3
IA-775
A 1 .2
CH(CH 3 )CH 2 CH 3
CH 2 CH 3
IA-776
A 1 .2
CH 2 CHCH 2
CH 2 CH 3
IA-777
A 1 .2
CH 2 CCH
CH 2 CH 3
IA-778
A 1 .2
CH(CH 3 )CH═CH 2
CH 2 CH 3
IA-779
A 1 .2
CHF 2
CH 2 CH 3
IA-780
A 1 .2
CH 2 Cl
CH 2 CH 3
IA-781
A 1 .2
CH 2 CH 2 CN
CH 2 CH 3
IA-782
A 1 .2
CH 2 CH 2 Cl
CH 2 CH 3
IA-783
A 1 .2
CH 2 CH 2 OH
CH 2 CH 3
IA-784
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 3
IA-785
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 3
IA-786
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 3
IA-787
A 1 .2
CH 2 SCH 3
CH 2 CH 3
IA-788
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 3
IA-789
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 3
IA-790
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 3
IA-791
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 3
IA-792
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 3
IA-793
A 1 .2
CH 2 COOH
CH 2 CH 3
IA-794
A 1 .2
CH 2 COOCH 3
CH 2 CH 3
IA-795
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 3
IA-796
A 1 .2
cyclo-C 3 H 5
CH 2 CH 3
IA-797
A 1 .2
cyclo-C 4 H 7
CH 2 CH 3
IA-798
A 1 .2
cyclo-C 5 H 9
CH 2 CH 3
IA-799
A 1 .2
cyclo-C 6 H 11
CH 2 CH 3
IA-800
A 1 .2
C 6 H 5
CH 2 CH 3
IA-801
A 1 .2
CH═CH 2
CH═CH 2
IA-802
A 1 .2
CH 2 CH 2 CH 3
CH═CH 2
IA-803
A 1 .2
CH(CH 3 ) 2
CH═CH 2
IA-804
A 1 .2
CH 2 CH 2 CH 2 CH 3
CH═CH 2
IA-805
A 1 .2
C(CH 3 ) 3
CH═CH 2
IA-806
A 1 .2
CH 2 CH(CH 3 ) 2
CH═CH 2
IA-807
A 1 .2
CH(CH 3 )CH 2 CH 3
CH═CH 2
IA-808
A 1 .2
CH 2 CHCH 2
CH═CH 2
IA-809
A 1 .2
CH 2 CCH
CH═CH 2
IA-810
A 1 .2
CH(CH 3 )CH═CH 2
CH═CH 2
IA-811
A 1 .2
CHF 2
CH═CH 2
IA-812
A 1 .2
CH 2 Cl
CH═CH 2
IA-813
A 1 .2
CH 2 CH 2 CN
CH═CH 2
IA-814
A 1 .2
CH 2 CH 2 Cl
CH═CH 2
IA-815
A 1 .2
CH 2 CH 2 OH
CH═CH 2
IA-816
A 1 .2
CH 2 CH 2 CH 2 OH
CH═CH 2
IA-817
A 1 .2
CH 2 CH(OH)CH 2 OH
CH═CH 2
IA-818
A 1 .2
CH 2 CH(OCH 3 ) 2
CH═CH 2
IA-819
A 1 .2
CH 2 SCH 3
CH═CH 2
IA-820
A 1 .2
(CH 2 ) 3 SCH 3
CH═CH 2
IA-821
A 1 .2
CH 2 S(═O)CH 3
CH═CH 2
IA-822
A 1 .2
CH 2 S(═O) 2 CH 3
CH═CH 2
IA-823
A 1 .2
CH 2 C(═O)CH 3
CH═CH 2
IA-824
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH═CH 2
IA-825
A 1 .2
CH 2 COOH
CH═CH 2
IA-826
A 1 .2
CH 2 COOCH 3
CH═CH 2
IA-827
A 1 .2
CH 2 COOCH 2 CH 3
CH═CH 2
IA-828
A 1 .2
cyclo-C 3 H 5
CH═CH 2
IA-829
A 1 .2
cyclo-C 4 H 7
CH═CH 2
IA-830
A 1 .2
cyclo-C 5 H 9
CH═CH 2
IA-831
A 1 .2
cyclo-C 6 H 11
CH═CH 2
IA-832
A 1 .2
C 6 H 5
CH═CH 2
IA-833
A 1 .2
CH 2 CH 2 CH 3
CH 2 CH 2 CH 3
IA-834
A 1 .2
CH(CH 3 ) 2
CH 2 CH 2 CH 3
IA-835
A 1 .2
CH 2 CH 2 CH 2 CH 3
CH 2 CH 2 CH 3
IA-836
A 1 .2
C(CH 3 ) 3
CH 2 CH 2 CH 3
IA-837
A 1 .2
CH 2 CH(CH 3 ) 2
CH 2 CH 2 CH 3
IA-838
A 1 .2
CH(CH 3 )CH 2 CH 3
CH 2 CH 2 CH 3
IA-839
A 1 .2
CH 2 CHCH 2
CH 2 CH 2 CH 3
IA-840
A 1 .2
CH 2 CCH
CH 2 CH 2 CH 3
IA-841
A 1 .2
CH(CH 3 )CH═CH 2
CH 2 CH 2 CH 3
IA-842
A 1 .2
CHF 2
CH 2 CH 2 CH 3
IA-843
A 1 .2
CH 2 Cl
CH 2 CH 2 CH 3
IA-844
A 1 .2
CH 2 CH 2 CN
CH 2 CH 2 CH 3
IA-845
A 1 .2
CH 2 CH 2 Cl
CH 2 CH 2 CH 3
IA-846
A 1 .2
CH 2 CH 2 OH
CH 2 CH 2 CH 3
IA-847
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CH 3
IA-848
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CH 3
IA-849
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CH 3
IA-850
A 1 .2
CH 2 SCH 3
CH 2 CH 2 CH 3
IA-851
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 2 CH 3
IA-852
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 2 CH 3
IA-853
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CH 3
IA-854
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 2 CH 3
IA-855
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CH 3
IA-856
A 1 .2
CH 2 COOH
CH 2 CH 2 CH 3
IA-857
A 1 .2
CH 2 COOCH 3
CH 2 CH 2 CH 3
IA-858
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 2 CH 3
IA-859
A 1 .2
cyclo-C 3 H 5
CH 2 CH 2 CH 3
IA-860
A 1 .2
cyclo-C 4 H 7
CH 2 CH 2 CH 3
IA-861
A 1 .2
cyclo-C 5 H 9
CH 2 CH 2 CH 3
IA-862
A 1 .2
cyclo-C 6 H 11
CH 2 CH 2 CH 3
IA-863
A 1 .2
C 6 H 5
CH 2 CH 2 CH 3
IA-864
A 1 .2
CH(CH 3 ) 2
CH(CH 3 ) 2
IA-865
A 1 .2
CH 2 CH 2 CH 2 CH 3
CH(CH 3 ) 2
IA-866
A 1 .2
C(CH 3 ) 3
CH(CH 3 ) 2
IA-867
A 1 .2
CH 2 CH(CH 3 ) 2
CH(CH 3 ) 2
IA-868
A 1 .2
CH(CH 3 )CH 2 CH 3
CH(CH 3 ) 2
IA-869
A 1 .2
CH 2 CHCH 2
CH(CH 3 ) 2
IA-870
A 1 .2
CH 2 CCH
CH(CH 3 ) 2
IA-871
A 1 .2
CH(CH 3 )CH═CH 2
CH(CH 3 ) 2
IA-872
A 1 .2
CHF 2
CH(CH 3 ) 2
IA-873
A 1 .2
CH 2 Cl
CH(CH 3 ) 2
IA-874
A 1 .2
CH 2 CH 2 CN
CH(CH 3 ) 2
IA-875
A 1 .2
CH 2 CH 2 Cl
CH(CH 3 ) 2
IA-876
A 1 .2
CH 2 CH 2 OH
CH(CH 3 ) 2
IA-877
A 1 .2
CH 2 CH 2 CH 2 OH
CH(CH 3 ) 2
IA-878
A 1 .2
CH 2 CH(OH)CH 2 OH
CH(CH 3 ) 2
IA-879
A 1 .2
CH 2 CH(OCH 3 ) 2
CH(CH 3 ) 2
IA-880
A 1 .2
CH 2 SCH 3
CH(CH 3 ) 2
IA-881
A 1 .2
(CH 2 ) 3 SCH 3
CH(CH 3 ) 2
IA-882
A 1 .2
CH 2 S(═O)CH 3
CH(CH 3 ) 2
IA-883
A 1 .2
CH 2 S(═O) 2 CH 3
CH(CH 3 ) 2
IA-884
A 1 .2
CH 2 C(═O)CH 3
CH(CH 3 ) 2
IA-885
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH(CH 3 ) 2
IA-886
A 1 .2
CH 2 COOH
CH(CH 3 ) 2
IA-887
A 1 .2
CH 2 COOCH 3
CH(CH 3 ) 2
IA-888
A 1 .2
CH 2 COOCH 2 CH 3
CH(CH 3 ) 2
IA-889
A 1 .2
cyclo-C 3 H 5
CH(CH 3 ) 2
IA-890
A 1 .2
cyclo-C 4 H 7
CH(CH 3 ) 2
IA-891
A 1 .2
cyclo-C 5 H 9
CH(CH 3 ) 2
IA-892
A 1 .2
cyclo-C 6 H 11
CH(CH 3 ) 2
IA-893
A 1 .2
C 6 H 5
CH(CH 3 ) 2
IA-894
A 1 .2
CH 2 CH 2 CH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-895
A 1 .2
C(CH 3 ) 3
CH 2 CH 2 CH 2 CH 3
IA-896
A 1 .2
CH 2 CH(CH 3 ) 2
CH 2 CH 2 CH 2 CH 3
IA-897
A 1 .2
CH(CH 3 )CH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-898
A 1 .2
CH 2 CHCH 2
CH 2 CH 2 CH 2 CH 3
IA-899
A 1 .2
CH 2 CCH
CH 2 CH 2 CH 2 CH 3
IA-900
A 1 .2
CH(CH 3 )CH═CH 2
CH 2 CH 2 CH 2 CH 3
IA-901
A 1 .2
CHF 2
CH 2 CH 2 CH 2 CH 3
IA-902
A 1 .2
CH 2 Cl
CH 2 CH 2 CH 2 CH 3
IA-903
A 1 .2
CH 2 CH 2 CN
CH 2 CH 2 CH 2 CH 3
IA-904
A 1 .2
CH 2 CH 2 Cl
CH 2 CH 2 CH 2 CH 3
IA-905
A 1 .2
CH 2 CH 2 OH
CH 2 CH 2 CH 2 CH 3
IA-906
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CH 2 CH 3
IA-907
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CH 2 CH 3
IA-908
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CH 2 CH 3
IA-909
A 1 .2
CH 2 SCH 3
CH 2 CH 2 CH 2 CH 3
IA-910
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 2 CH 2 CH 3
IA-911
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 2 CH 2 CH 3
IA-912
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-913
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 2 CH 2 CH 3
IA-914
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-915
A 1 .2
CH 2 COOH
CH 2 CH 2 CH 2 CH 3
IA-916
A 1 .2
CH 2 COOCH 3
CH 2 CH 2 CH 2 CH 3
IA-917
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 2 CH 2 CH 3
IA-918
A 1 .2
cyclo-C 3 H 5
CH 2 CH 2 CH 2 CH 3
IA-919
A 1 .2
cyclo-C 4 H 7
CH 2 CH 2 CH 2 CH 3
IA-920
A 1 .2
cyclo-C 5 H 9
CH 2 CH 2 CH 2 CH 3
IA-921
A 1 .2
cyclo-C 6 H 11
CH 2 CH 2 CH 2 CH 3
IA-922
A 1 .2
C 6 H 5
CH 2 CH 2 CH 2 CH 3
IA-923
A 1 .2
C(CH 3 ) 3
C(CH 3 ) 3
IA-924
A 1 .2
CH 2 CH(CH 3 ) 2
C(CH 3 ) 3
IA-925
A 1 .2
CH(CH 3 )CH 2 CH 3
C(CH 3 ) 3
IA-926
A 1 .2
CH 2 CHCH 2
C(CH 3 ) 3
IA-927
A 1 .2
CH 2 CCH
C(CH 3 ) 3
IA-928
A 1 .2
CH(CH 3 )CH═CH 2
C(CH 3 ) 3
IA-929
A 1 .2
CHF 2
C(CH 3 ) 3
IA-930
A 1 .2
CH 2 Cl
C(CH 3 ) 3
IA-931
A 1 .2
CH 2 CH 2 CN
C(CH 3 ) 3
IA-932
A 1 .2
CH 2 CH 2 Cl
C(CH 3 ) 3
IA-933
A 1 .2
CH 2 CH 2 OH
C(CH 3 ) 3
IA-934
A 1 .2
CH 2 CH 2 CH 2 OH
C(CH 3 ) 3
IA-935
A 1 .2
CH 2 CH(OH)CH 2 OH
C(CH 3 ) 3
IA-936
A 1 .2
CH 2 CH(OCH 3 ) 2
C(CH 3 ) 3
IA-937
A 1 .2
CH 2 SCH 3
C(CH 3 ) 3
IA-938
A 1 .2
(CH 2 ) 3 SCH 3
C(CH 3 ) 3
IA-939
A 1 .2
CH 2 S(═O)CH 3
C(CH 3 ) 3
IA-940
A 1 .2
CH 2 S(═O) 2 CH 3
C(CH 3 ) 3
IA-941
A 1 .2
CH 2 C(═O)CH 3
C(CH 3 ) 3
IA-942
A 1 .2
CH 2 C(═O)CH 2 CH 3
C(CH 3 ) 3
IA-943
A 1 .2
CH 2 COOH
C(CH 3 ) 3
IA-944
A 1 .2
CH 2 COOCH 3
C(CH 3 ) 3
IA-945
A 1 .2
CH 2 COOCH 2 CH 3
C(CH 3 ) 3
IA-946
A 1 .2
cyclo-C 3 H 5
C(CH 3 ) 3
IA-947
A 1 .2
cyclo-C 4 H 7
C(CH 3 ) 3
IA-948
A 1 .2
cyclo-C 5 H 9
C(CH 3 ) 3
IA-949
A 1 .2
cyclo-C 6 H 11
C(CH 3 ) 3
IA-950
A 1 .2
C 6 H 5
C(CH 3 ) 3
IA-951
A 1 .2
CH 2 CH(CH 3 ) 2
CH 2 CH(CH 3 ) 2
IA-952
A 1 .2
CH(CH 3 )CH 2 CH 3
CH 2 CH(CH 3 ) 2
IA-953
A 1 .2
CH 2 CHCH 2
CH 2 CH(CH 3 ) 2
IA-954
A 1 .2
CH 2 CCH
CH 2 CH(CH 3 ) 2
IA-955
A 1 .2
CH(CH 3 )CH═CH 2
CH 2 CH(CH 3 ) 2
IA-956
A 1 .2
CHF 2
CH 2 CH(CH 3 ) 2
IA-957
A 1 .2
CH 2 Cl
CH 2 CH(CH 3 ) 2
IA-958
A 1 .2
CH 2 CH 2 CN
CH 2 CH(CH 3 ) 2
IA-959
A 1 .2
CH 2 CH 2 Cl
CH 2 CH(CH 3 ) 2
IA-960
A 1 .2
CH 2 CH 2 OH
CH 2 CH(CH 3 ) 2
IA-961
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH(CH 3 ) 2
IA-962
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH(CH 3 ) 2
IA-963
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH(CH 3 ) 2
IA-964
A 1 .2
CH 2 SCH 3
CH 2 CH(CH 3 ) 2
IA-965
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH(CH 3 ) 2
IA-966
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH(CH 3 ) 2
IA-967
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH(CH 3 ) 2
IA-968
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH(CH 3 ) 2
IA-969
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH(CH 3 ) 2
IA-970
A 1 .2
CH 2 COOH
CH 2 CH(CH 3 ) 2
IA-971
A 1 .2
CH 2 COOCH 3
CH 2 CH(CH 3 ) 2
IA-972
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH(CH 3 ) 2
IA-973
A 1 .2
cyclo-C 3 H 5
CH 2 CH(CH 3 ) 2
IA-974
A 1 .2
cyclo-C 4 H 7
CH 2 CH(CH 3 ) 2
IA-975
A 1 .2
cyclo-C 5 H 9
CH 2 CH(CH 3 ) 2
IA-976
A 1 .2
cyclo-C 6 H 11
CH 2 CH(CH 3 ) 2
IA-977
A 1 .2
C 6 H 5
CH 2 CH(CH 3 ) 2
IA-978
A 1 .2
CH(CH 3 )CH 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-979
A 1 .2
CH 2 CHCH 2
CH(CH 3 )CH 2 CH 3
IA-980
A 1 .2
CH 2 CCH
CH(CH 3 )CH 2 CH 3
IA-981
A 1 .2
CH(CH 3 )CH═CH 2
CH(CH 3 )CH 2 CH 3
IA-982
A 1 .2
CHF 2
CH(CH 3 )CH 2 CH 3
IA-983
A 1 .2
CH 2 Cl
CH(CH 3 )CH 2 CH 3
IA-984
A 1 .2
CH 2 CH 2 CN
CH(CH 3 )CH 2 CH 3
IA-985
A 1 .2
CH 2 CH 2 Cl
CH(CH 3 )CH 2 CH 3
IA-986
A 1 .2
CH 2 CH 2 OH
CH(CH 3 )CH 2 CH 3
IA-987
A 1 .2
CH 2 CH 2 CH 2 OH
CH(CH 3 )CH 2 CH 3
IA-988
A 1 .2
CH 2 CH(OH)CH 2 OH
CH(CH 3 )CH 2 CH 3
IA-989
A 1 .2
CH 2 CH(OCH 3 ) 2
CH(CH 3 )CH 2 CH 3
IA-990
A 1 .2
CH 2 SCH 3
CH(CH 3 )CH 2 CH 3
IA-991
A 1 .2
(CH 2 ) 3 SCH 3
CH(CH 3 )CH 2 CH 3
IA-992
A 1 .2
CH 2 S(═O)CH 3
CH(CH 3 )CH 2 CH 3
IA-993
A 1 .2
CH 2 S(═O) 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-994
A 1 .2
CH 2 C(═O)CH 3
CH(CH 3 )CH 2 CH 3
IA-995
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-996
A 1 .2
CH 2 COOH
CH(CH 3 )CH 2 CH 3
IA-997
A 1 .2
CH 2 COOCH 3
CH(CH 3 )CH 2 CH 3
IA-998
A 1 .2
CH 2 COOCH 2 CH 3
CH(CH 3 )CH 2 CH 3
IA-999
A 1 .2
cyclo-C 3 H 5
CH(CH 3 )CH 2 CH 3
IA-1000
A 1 .2
cyclo-C 4 H 7
CH(CH 3 )CH 2 CH 3
IA-1001
A 1 .2
cyclo-C 5 H 9
CH(CH 3 )CH 2 CH 3
IA-1002
A 1 .2
cyclo-C 6 H 11
CH(CH 3 )CH 2 CH 3
IA-1003
A 1 .2
C 6 H 5
CH(CH 3 )CH 2 CH 3
IA-1004
A 1 .2
CH 2 CHCH 2
CH 2 CHCH 2
IA-1005
A 1 .2
CH 2 CCH
CH 2 CHCH 2
IA-1006
A 1 .2
CH(CH 3 )CH═CH 2
CH 2 CHCH 2
IA-1007
A 1 .2
CHF 2
CH 2 CHCH 2
IA-1008
A 1 .2
CH 2 Cl
CH 2 CHCH 2
IA-1009
A 1 .2
CH 2 CH 2 CN
CH 2 CHCH 2
IA-1010
A 1 .2
CH 2 CH 2 Cl
CH 2 CHCH 2
IA-1011
A 1 .2
CH 2 CH 2 OH
CH 2 CHCH 2
IA-1012
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CHCH 2
IA-1013
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CHCH 2
IA-1014
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CHCH 2
IA-1015
A 1 .2
CH 2 SCH 3
CH 2 CHCH 2
IA-1016
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CHCH 2
IA-1017
A 1 .2
CH 2 S(═O)CH 3
CH 2 CHCH 2
IA-1018
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CHCH 2
IA-1019
A 1 .2
CH 2 C(═O)CH 3
CH 2 CHCH 2
IA-1020
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CHCH 2
IA-1021
A 1 .2
CH 2 COOH
CH 2 CHCH 2
IA-1022
A 1 .2
CH 2 COOCH 3
CH 2 CHCH 2
IA-1023
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CHCH 2
IA-1024
A 1 .2
cyclo-C 3 H 5
CH 2 CHCH 2
IA-1025
A 1 .2
cyclo-C 4 H 7
CH 2 CHCH 2
IA-1026
A 1 .2
cyclo-C 5 H 9
CH 2 CHCH 2
IA-1027
A 1 .2
cyclo-C 6 H 11
CH 2 CHCH 2
IA-1028
A 1 .2
C 6 H 5
CH 2 CHCH 2
IA-1029
A 1 .2
CH 2 CCH
CH 2 CCH
IA-1030
A 1 .2
CH(CH 3 )CH═CH 2
CH 2 CCH
IA-1031
A 1 .2
CHF 2
CH 2 CCH
IA-1032
A 1 .2
CH 2 Cl
CH 2 CCH
IA-1033
A 1 .2
CH 2 CH 2 CN
CH 2 CCH
IA-1034
A 1 .2
CH 2 CH 2 Cl
CH 2 CCH
IA-1035
A 1 .2
CH 2 CH 2 OH
CH 2 CCH
IA-1036
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CCH
IA-1037
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CCH
IA-1038
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CCH
IA-1039
A 1 .2
CH 2 SCH 3
CH 2 CCH
IA-1040
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CCH
IA-1041
A 1 .2
CH 2 S(═O)CH 3
CH 2 CCH
IA-1042
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CCH
IA-1043
A 1 .2
CH 2 C(═O)CH 3
CH 2 CCH
IA-1044
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CCH
IA-1045
A 1 .2
CH 2 COOH
CH 2 CCH
IA-1046
A 1 .2
CH 2 COOCH 3
CH 2 CCH
IA-1047
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CCH
IA-1048
A 1 .2
cyclo-C 3 H 5
CH 2 CCH
IA-1049
A 1 .2
cyclo-C 4 H 7
CH 2 CCH
IA-1050
A 1 .2
cyclo-C 5 H 9
CH 2 CCH
IA-1051
A 1 .2
cyclo-C 6 H 11
CH 2 CCH
IA-1052
A 1 .2
C 6 H 5
CH 2 CCH
IA-1053
A 1 .2
CH(CH 3 )CH═CH 2
CH(CH 3 )CH═CH 2
IA-1054
A 1 .2
CHF 2
CH(CH 3 )CH═CH 2
IA-1055
A 1 .2
CH 2 Cl
CH(CH 3 )CH═CH 2
IA-1056
A 1 .2
CH 2 CH 2 CN
CH(CH 3 )CH═CH 2
IA-1057
A 1 .2
CH 2 CH 2 Cl
CH(CH 3 )CH═CH 2
IA-1058
A 1 .2
CH 2 CH 2 OH
CH(CH 3 )CH═CH 2
IA-1059
A 1 .2
CH 2 CH 2 CH 2 OH
CH(CH 3 )CH═CH 2
IA-1060
A 1 .2
CH 2 CH(OH)CH 2 OH
CH(CH 3 )CH═CH 2
IA-1061
A 1 .2
CH 2 CH(OCH 3 ) 2
CH(CH 3 )CH═CH 2
IA-1062
A 1 .2
CH 2 SCH 3
CH(CH 3 )CH═CH 2
IA-1063
A 1 .2
(CH 2 ) 3 SCH 3
CH(CH 3 )CH═CH 2
IA-1064
A 1 .2
CH 2 S(═O)CH 3
CH(CH 3 )CH═CH 2
IA-1065
A 1 .2
CH 2 S(═O) 2 CH 3
CH(CH 3 )CH═CH 2
IA-1066
A 1 .2
CH 2 C(═O)CH 3
CH(CH 3 )CH═CH 2
IA-1067
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH(CH 3 )CH═CH 2
IA-1068
A 1 .2
CH 2 COOH
CH(CH 3 )CH═CH 2
IA-1069
A 1 .2
CH 2 COOCH 3
CH(CH 3 )CH═CH 2
IA-1070
A 1 .2
CH 2 COOCH 2 CH 3
CH(CH 3 )CH═CH 2
IA-1071
A 1 .2
cyclo-C 3 H 5
CH(CH 3 )CH═CH 2
IA-1072
A 1 .2
cyclo-C 4 H 7
CH(CH 3 )CH═CH 2
IA-1073
A 1 .2
cyclo-C 5 H 9
CH(CH 3 )CH═CH 2
IA-1074
A 1 .2
cyclo-C 6 H 11
CH(CH 3 )CH═CH 2
IA-1075
A 1 .2
C 6 H 5
CH(CH 3 )CH═CH 2
IA-1076
A 1 .2
CHF 2
CHF 2
IA-1077
A 1 .2
CH 2 Cl
CHF 2
IA-1078
A 1 .2
CH 2 CH 2 CN
CHF 2
IA-1079
A 1 .2
CH 2 CH 2 Cl
CHF 2
IA-1080
A 1 .2
CH 2 CH 2 OH
CHF 2
IA-1081
A 1 .2
CH 2 CH 2 CH 2 OH
CHF 2
IA-1082
A 1 .2
CH 2 CH(OH)CH 2 OH
CHF 2
IA-1083
A 1 .2
CH 2 CH(OCH 3 ) 2
CHF 2
IA-1084
A 1 .2
CH 2 SCH 3
CHF 2
IA-1085
A 1 .2
(CH 2 ) 3 SCH 3
CHF 2
IA-1086
A 1 .2
CH 2 S(═O)CH 3
CHF 2
IA-1087
A 1 .2
CH 2 S(═O) 2 CH 3
CHF 2
IA-1088
A 1 .2
CH 2 C(═O)CH 3
CHF 2
IA-1089
A 1 .2
CH 2 C(═O)CH 2 CH 3
CHF 2
IA-1090
A 1 .2
CH 2 COOH
CHF 2
IA-1091
A 1 .2
CH 2 COOCH 3
CHF 2
IA-1092
A 1 .2
CH 2 COOCH 2 CH 3
CHF 2
IA-1093
A 1 .2
cyclo-C 3 H 5
CHF 2
IA-1094
A 1 .2
cyclo-C 4 H 7
CHF 2
IA-1095
A 1 .2
cyclo-C 5 H 9
CHF 2
IA-1096
A 1 .2
cyclo-C 6 H 11
CHF 2
IA-1097
A 1 .2
C 6 H 5
CHF 2
IA-1098
A 1 .2
CH 2 Cl
CH 2 Cl
IA-1099
A 1 .2
CH 2 CH 2 CN
CH 2 Cl
IA-1100
A 1 .2
CH 2 CH 2 Cl
CH 2 Cl
IA-1101
A 1 .2
CH 2 CH 2 OH
CH 2 Cl
IA-1102
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 Cl
IA-1103
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 Cl
IA-1104
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 Cl
IA-1105
A 1 .2
CH 2 SCH 3
CH 2 Cl
IA-1106
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 Cl
IA-1107
A 1 .2
CH 2 S(═O)CH 3
CH 2 Cl
IA-1108
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 Cl
IA-1109
A 1 .2
CH 2 C(═O)CH 3
CH 2 Cl
IA-1110
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 Cl
IA-1111
A 1 .2
CH 2 COOH
CH 2 Cl
IA-1112
A 1 .2
CH 2 COOCH 3
CH 2 Cl
IA-1113
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 Cl
IA-1114
A 1 .2
cyclo-C 3 H 5
CH 2 Cl
IA-1115
A 1 .2
cyclo-C 4 H 7
CH 2 Cl
IA-1116
A 1 .2
cyclo-C 5 H 9
CH 2 Cl
IA-1117
A 1 .2
cyclo-C 6 H 11
CH 2 Cl
IA-1118
A 1 .2
C 6 H 5
CH 2 Cl
IA-1119
A 1 .2
CH 2 CH 2 CN
CH 2 CH 2 CN
IA-1120
A 1 .2
CH 2 CH 2 Cl
CH 2 CH 2 CN
IA-1121
A 1 .2
CH 2 CH 2 OH
CH 2 CH 2 CN
IA-1122
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CN
IA-1123
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CN
IA-1124
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CN
IA-1125
A 1 .2
CH 2 SCH 3
CH 2 CH 2 CN
IA-1126
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 2 CN
IA-1127
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 2 CN
IA-1128
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CN
IA-1129
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 2 CN
IA-1130
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CN
IA-1131
A 1 .2
CH 2 COOH
CH 2 CH 2 CN
IA-1132
A 1 .2
CH 2 COOCH 3
CH 2 CH 2 CN
IA-1133
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 2 CN
IA-1134
A 1 .2
cyclo-C 3 H 5
CH 2 CH 2 CN
IA-1135
A 1 .2
cyclo-C 4 H 7
CH 2 CH 2 CN
IA-1136
A 1 .2
cyclo-C 5 H 9
CH 2 CH 2 CN
IA-1137
A 1 .2
cyclo-C 6 H 11
CH 2 CH 2 CN
IA-1138
A 1 .2
C 6 H 5
CH 2 CH 2 CN
IA-1139
A 1 .2
CH 2 CH 2 Cl
CH 2 CH 2 Cl
IA-1140
A 1 .2
CH 2 CH 2 OH
CH 2 CH 2 Cl
IA-1141
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 2 Cl
IA-1142
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 Cl
IA-1143
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 Cl
IA-1144
A 1 .2
CH 2 SCH 3
CH 2 CH 2 Cl
IA-1145
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 2 Cl
IA-1146
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 2 Cl
IA-1147
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 2 Cl
IA-1148
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 2 Cl
IA-1149
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 Cl
IA-1150
A 1 .2
CH 2 COOH
CH 2 CH 2 Cl
IA-1151
A 1 .2
CH 2 COOCH 3
CH 2 CH 2 Cl
IA-1152
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 2 Cl
IA-1153
A 1 .2
cyclo-C 3 H 5
CH 2 CH 2 Cl
IA-1154
A 1 .2
cyclo-C 4 H 7
CH 2 CH 2 Cl
IA-1155
A 1 .2
cyclo-C 5 H 9
CH 2 CH 2 Cl
IA-1156
A 1 .2
cyclo-C 6 H 11
CH 2 CH 2 Cl
IA-1157
A 1 .2
C 6 H 5
CH 2 CH 2 Cl
IA-1158
A 1 .2
CH 2 CH 2 OH
CH 2 CH 2 OH
IA-1159
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 2 OH
IA-1160
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 OH
IA-1161
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 OH
IA-1162
A 1 .2
CH 2 SCH 3
CH 2 CH 2 OH
IA-1163
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 2 OH
IA-1164
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 2 OH
IA-1165
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 2 OH
IA-1166
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 2 OH
IA-1167
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 OH
IA-1168
A 1 .2
CH 2 COOH
CH 2 CH 2 OH
IA-1169
A 1 .2
CH 2 COOCH 3
CH 2 CH 2 OH
IA-1170
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 2 OH
IA-1171
A 1 .2
cyclo-C 3 H 5
CH 2 CH 2 OH
IA-1172
A 1 .2
cyclo-C 4 H 7
CH 2 CH 2 OH
IA-1173
A 1 .2
cyclo-C 5 H 9
CH 2 CH 2 OH
IA-1174
A 1 .2
cyclo-C 6 H 11
CH 2 CH 2 OH
IA-1175
A 1 .2
C 6 H 5
CH 2 CH 2 OH
IA-1176
A 1 .2
CH 2 CH 2 CH 2 OH
CH 2 CH 2 CH 2 OH
IA-1177
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH 2 CH 2 OH
IA-1178
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH 2 CH 2 OH
IA-1179
A 1 .2
CH 2 SCH 3
CH 2 CH 2 CH 2 OH
IA-1180
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH 2 CH 2 OH
IA-1181
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH 2 CH 2 OH
IA-1182
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH 2 CH 2 OH
IA-1183
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH 2 CH 2 OH
IA-1184
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH 2 CH 2 OH
IA-1185
A 1 .2
CH 2 COOH
CH 2 CH 2 CH 2 OH
IA-1186
A 1 .2
CH 2 COOCH 3
CH 2 CH 2 CH 2 OH
IA-1187
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH 2 CH 2 OH
IA-1188
A 1 .2
cyclo-C 3 H 5
CH 2 CH 2 CH 2 OH
IA-1189
A 1 .2
cyclo-C 4 H 7
CH 2 CH 2 CH 2 OH
IA-1190
A 1 .2
cyclo-C 5 H 9
CH 2 CH 2 CH 2 OH
IA-1191
A 1 .2
cyclo-C 6 H 11
CH 2 CH 2 CH 2 OH
IA-1192
A 1 .2
C 6 H 5
CH 2 CH 2 CH 2 OH
IA-1193
A 1 .2
CH 2 CH(OH)CH 2 OH
CH 2 CH(OH)CH 2 OH
IA-1194
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH(OH)CH 2 OH
IA-1195
A 1 .2
CH 2 SCH 3
CH 2 CH(OH)CH 2 OH
IA-1196
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH(OH)CH 2 OH
IA-1197
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH(OH)CH 2 OH
IA-1198
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH(OH)CH 2 OH
IA-1199
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH(OH)CH 2 OH
IA-1200
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH(OH)CH 2 OH
IA-1201
A 1 .2
CH 2 COOH
CH 2 CH(OH)CH 2 OH
IA-1202
A 1 .2
CH 2 COOCH 3
CH 2 CH(OH)CH 2 OH
IA-1203
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH(OH)CH 2 OH
IA-1204
A 1 .2
cyclo-C 3 H 5
CH 2 CH(OH)CH 2 OH
IA-1205
A 1 .2
cyclo-C 4 H 7
CH 2 CH(OH)CH 2 OH
IA-1206
A 1 .2
cyclo-C 5 H 9
CH 2 CH(OH)CH 2 OH
IA-1207
A 1 .2
cyclo-C 6 H 11
CH 2 CH(OH)CH 2 OH
IA-1208
A 1 .2
C 6 H 5
CH 2 CH(OH)CH 2 OH
IA-1209
A 1 .2
CH 2 CH(OCH 3 ) 2
CH 2 CH(OCH 3 ) 2
IA-1210
A 1 .2
CH 2 SCH 3
CH 2 CH(OCH 3 ) 2
IA-1211
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 CH(OCH 3 ) 2
IA-1212
A 1 .2
CH 2 S(═O)CH 3
CH 2 CH(OCH 3 ) 2
IA-1213
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 CH(OCH 3 ) 2
IA-1214
A 1 .2
CH 2 C(═O)CH 3
CH 2 CH(OCH 3 ) 2
IA-1215
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 CH(OCH 3 ) 2
IA-1216
A 1 .2
CH 2 COOH
CH 2 CH(OCH 3 ) 2
IA-1217
A 1 .2
CH 2 COOCH 3
CH 2 CH(OCH 3 ) 2
IA-1218
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 CH(OCH 3 ) 2
IA-1219
A 1 .2
cyclo-C 3 H 5
CH 2 CH(OCH 3 ) 2
IA-1220
A 1 .2
cyclo-C 4 H 7
CH 2 CH(OCH 3 ) 2
IA-1221
A 1 .2
cyclo-C 5 H 9
CH 2 CH(OCH 3 ) 2
IA-1222
A 1 .2
cyclo-C 6 H 11
CH 2 CH(OCH 3 ) 2
IA-1223
A 1 .2
C 6 H 5
CH 2 CH(OCH 3 ) 2
IA-1224
A 1 .2
CH 2 SCH 3
CH 2 SCH 3
IA-1225
A 1 .2
(CH 2 ) 3 SCH 3
CH 2 SCH 3
IA-1226
A 1 .2
CH 2 S(═O)CH 3
CH 2 SCH 3
IA-1227
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 SCH 3
IA-1228
A 1 .2
CH 2 C(═O)CH 3
CH 2 SCH 3
IA-1229
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 SCH 3
IA-1230
A 1 .2
CH 2 COOH
CH 2 SCH 3
IA-1231
A 1 .2
CH 2 COOCH 3
CH 2 SCH 3
IA-1232
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 SCH 3
IA-1233
A 1 .2
cyclo-C 3 H 5
CH 2 SCH 3
IA-1234
A 1 .2
cyclo-C 4 H 7
CH 2 SCH 3
IA-1235
A 1 .2
cyclo-C 5 H 9
CH 2 SCH 3
IA-1236
A 1 .2
cyclo-C 6 H 11
CH 2 SCH 3
IA-1237
A 1 .2
C 6 H 5
CH 2 SCH 3
IA-1238
A 1 .2
(CH 2 ) 3 SCH 3
(CH 2 ) 3 SCH 3
IA-1239
A 1 .2
CH 2 S(═O)CH 3
(CH 2 ) 3 SCH 3
IA-1240
A 1 .2
CH 2 S(═O) 2 CH 3
(CH 2 ) 3 SCH 3
IA-1241
A 1 .2
CH 2 C(═O)CH 3
(CH 2 ) 3 SCH 3
IA-1242
A 1 .2
CH 2 C(═O)CH 2 CH 3
(CH 2 ) 3 SCH 3
IA-1243
A 1 .2
CH 2 COOH
(CH 2 ) 3 SCH 3
IA-1244
A 1 .2
CH 2 COOCH 3
(CH 2 ) 3 SCH 3
IA-1245
A 1 .2
CH 2 COOCH 2 CH 3
(CH 2 ) 3 SCH 3
IA-1246
A 1 .2
cyclo-C 3 H 5
(CH 2 ) 3 SCH 3
IA-1247
A 1 .2
cyclo-C 4 H 7
(CH 2 ) 3 SCH 3
IA-1248
A 1 .2
cyclo-C 5 H 9
(CH 2 ) 3 SCH 3
IA-1249
A 1 .2
cyclo-C 6 H 11
(CH 2 ) 3 SCH 3
IA-1250
A 1 .2
C 6 H 5
(CH 2 ) 3 SCH 3
IA-1251
A 1 .2
CH 2 S(═O)CH 3
CH 2 S(═O)CH 3
IA-1252
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 S(═O)CH 3
IA-1253
A 1 .2
CH 2 C(═O)CH 3
CH 2 S(═O)CH 3
IA-1254
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 S(═O)CH 3
IA-1255
A 1 .2
CH 2 COOH
CH 2 S(═O)CH 3
IA-1256
A 1 .2
CH 2 COOCH 3
CH 2 S(═O)CH 3
IA-1257
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 S(═O)CH 3
IA-1258
A 1 .2
cyclo-C 3 H 5
CH 2 S(═O)CH 3
IA-1259
A 1 .2
cyclo-C 4 H 7
CH 2 S(═O)CH 3
IA-1260
A 1 .2
cyclo-C 5 H 9
CH 2 S(═O)CH 3
IA-1261
A 1 .2
cyclo-C 6 H 11
CH 2 S(═O)CH 3
IA-1262
A 1 .2
C 6 H 5
CH 2 S(═O)CH 3
IA-1263
A 1 .2
CH 2 S(═O) 2 CH 3
CH 2 S(═O) 2 CH 3
IA-1264
A 1 .2
CH 2 C(═O)CH 3
CH 2 S(═O) 2 CH 3
IA-1265
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 S(═O) 2 CH 3
IA-1266
A 1 .2
CH 2 COOH
CH 2 S(═O) 2 CH 3
IA-1267
A 1 .2
CH 2 COOCH 3
CH 2 S(═O) 2 CH 3
IA-1268
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 S(═O) 2 CH 3
IA-1269
A 1 .2
cyclo-C 3 H 5
CH 2 S(═O) 2 CH 3
IA-1270
A 1 .2
cyclo-C 4 H 7
CH 2 S(═O) 2 CH 3
IA-1271
A 1 .2
cyclo-C 5 H 9
CH 2 S(═O) 2 CH 3
IA-1272
A 1 .2
cyclo-C 6 H 11
CH 2 S(═O) 2 CH 3
IA-1273
A 1 .2
C 6 H 5
CH 2 S(═O) 2 CH 3
IA-1274
A 1 .2
CH 2 C(═O)CH 3
CH 2 C(═O)CH 3
IA-1275
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 C(═O)CH 3
IA-1276
A 1 .2
CH 2 COOH
CH 2 C(═O)CH 3
IA-1277
A 1 .2
CH 2 COOCH 3
CH 2 C(═O)CH 3
IA-1278
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 C(═O)CH 3
IA-1279
A 1 .2
cyclo-C 3 H 5
CH 2 C(═O)CH 3
IA-1280
A 1 .2
cyclo-C 4 H 7
CH 2 C(═O)CH 3
IA-1281
A 1 .2
cyclo-C 5 H 9
CH 2 C(═O)CH 3
IA-1282
A 1 .2
cyclo-C 6 H 11
CH 2 C(═O)CH 3
IA-1283
A 1 .2
C 6 H 5
CH 2 C(═O)CH 3
IA-1284
A 1 .2
CH 2 C(═O)CH 2 CH 3
CH 2 C(═O)CH 2 CH 3
IA-1285
A 1 .2
CH 2 COOH
CH 2 C(═O)CH 2 CH 3
IA-1286
A 1 .2
CH 2 COOCH 3
CH 2 C(═O)CH 2 CH 3
IA-1287
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 C(═O)CH 2 CH 3
IA-1288
A 1 .2
cyclo-C 3 H 5
CH 2 C(═O)CH 2 CH 3
IA-1289
A 1 .2
cyclo-C 4 H 7
CH 2 C(═O)CH 2 CH 3
IA-1290
A 1 .2
cyclo-C 5 H 9
CH 2 C(═O)CH 2 CH 3
IA-1291
A 1 .2
cyclo-C 6 H 11
CH 2 C(═O)CH 2 CH 3
IA-1292
A 1 .2
C 6 H 5
CH 2 C(═O)CH 2 CH 3
IA-1293
A 1 .2
CH 2 COOH
CH 2 COOH
IA-1294
A 1 .2
CH 2 COOCH 3
CH 2 COOH
IA-1295
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 COOH
IA-1296
A 1 .2
cyclo-C 3 H 5
CH 2 COOH
IA-1297
A 1 .2
cyclo-C 4 H 7
CH 2 COOH
IA-1298
A 1 .2
cyclo-C 5 H 9
CH 2 COOH
IA-1299
A 1 .2
cyclo-C 6 H 11
CH 2 COOH
IA-1300
A 1 .2
C 6 H 5
CH 2 COOH
IA-1301
A 1 .2
CH 2 COOCH 3
CH 2 COOCH 3
IA-1302
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 COOCH 3
IA-1303
A 1 .2
cyclo-C 3 H 5
CH 2 COOCH 3
IA-1304
A 1 .2
cyclo-C 4 H 7
CH 2 COOCH 3
IA-1305
A 1 .2
cyclo-C 5 H 9
CH 2 COOCH 3
IA-1306
A 1 .2
cyclo-C 6 H 11
CH 2 COOCH 3
IA-1307
A 1 .2
C 6 H 5
CH 2 COOCH 3
IA-1308
A 1 .2
CH 2 COOCH 2 CH 3
CH 2 COOCH 2 CH 3
IA-1309
A 1 .2
cyclo-C 3 H 5
CH 2 COOCH 2 CH 3
IA-1310
A 1 .2
cyclo-C 4 H 7
CH 2 COOCH 2 CH 3
IA-1311
A 1 .2
cyclo-C 5 H 9
CH 2 COOCH 2 CH 3
IA-1312
A 1 .2
cyclo-C 6 H 11
CH 2 COOCH 2 CH 3
IA-1313
A 1 .2
C 6 H 5
CH 2 COOCH 2 CH 3
IA-1314
A 1 .2
cyclo-C 3 H 5
cyclo-C 3 H 5
IA-1315
A 1 .2
cyclo-C 4 H 7
cyclo-C 3 H 5
IA-1316
A 1 .2
cyclo-C 5 H 9
cyclo-C 3 H 5
IA-1317
A 1 .2
cyclo-C 6 H 11
cyclo-C 3 H 5
IA-1318
A 1 .2
C 6 H 5
cyclo-C 3 H 5
IA-1319
A 1 .2
cyclo-C 4 H 7
cyclo-C 4 H 7
IA-1320
A 1 .2
cyclo-C 5 H 9
cyclo-C 4 H 7
IA-1321
A 1 .2
cyclo-C 6 H 11
cyclo-C 4 H 7
IA-1322
A 1 .2
C 6 H 5
cyclo-C 4 H 7
IA-1323
A 1 .2
cyclo-C 5 H 9
cyclo-C 5 H 9
IA-1324
A 1 .2
cyclo-C 6 H 11
cyclo-C 5 H 9
IA-1325
A 1 .2
C 6 H 5
cyclo-C 5 H 9
IA-1326
A 1 .2
cyclo-C 6 H 11
cyclo-C 6 H 11
IA-1327
A 1 .2
C 6 H 5
cyclo-C 6 H 11
IA-1328
A 1 .2
C 6 H 5
C 6 H 5
and/or an enantiomer, a salt, and/or an N-oxide thereof.
7 : The compound of claim 6 , wherein R e and R f each independently are CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 or CH(CH 3 ) 2 .
8 : The compound of claim 6 ,
wherein Q 1 denotes chlorine; Q 3 denotes CF 3 ; and/or an enantiomer, a salt, and/or an N-oxide thereof.
9 : The compound of claim 8 , wherein R e and R f are CH 2 CH 3 .
10 : The compound of claim 8 , wherein R e and R f are CH(CH 3 ) 2 .
11 : The compound of claim 6 ,
wherein Q 1 denotes cyano; Q 3 denotes CF 3 ; and/or an enantiomer, a salt, and/or an N-oxide thereof.
12 : The compound of claim 11 , wherein R e and R f are CH(CH 3 ) 2 .
13 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of compound of formula I as defined in claim 2 .
14 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 6 .
15 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 7 .
16 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 8 .
17 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 9 .
18 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 10 .
19 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 11 .
20 : A method for the control of insects, acarids or nematodes by contacting the insect, acarid or nematode or their food supply, habitat, breeding ground or their locus with a pesticidally effective amount of a compound of formula I as defined in claim 12 .Join the waitlist — get patent alerts
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