Busqueda de Subestructura

CC=Cc1ccccc1

CCOC(=O)c1ccc(/C=C/c2cccc3c2C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #1466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)C(Sc1ccccc1)=CCC2(C)C
Reaction #1492
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC=C(Sc2ccccc2)c2cc(C(=O)O)ccc21
Reaction #1493
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(CN3CCN(CCO)CC3)c(=O)n(CC=Cc3ccc(Cl)cc3)n2)cc1F
Reaction #8133
title compound
Rendimiento 65.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10778
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC2Cc3ccc(C(=CC(=O)O)c4cccnc4)cc3C2)cc1
Reaction #50404
3-(2-(4-Toluenesulphonylamino)indan-5-yl)-3-(3-pyridyl)-prop-2-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)C(Sc1ccccc1)=CCC2(C)C
Reaction #52869
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC=C(Sc2ccccc2)c2cc(C(=O)O)ccc21
Reaction #52870
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2=C(CSc3ccccc32)C1=O
Reaction #62612
brown crystalline solid
Rendimiento 82.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccccc1C=C1CCOC1=O
Reaction #63158
title compound
Rendimiento 88.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2cccc(Cl)c2C=C2CCOC2=O)n1
Reaction #63160
title compound
Rendimiento 85.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccnc1-n1c(/C=C/c2ccccc2)nc2ccccc21.Cl
Reaction #79146
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1cccnc1-n1c(C=Cc2ccccc2)nc2ccccc21
Reaction #79148
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-n2c(/C=C/c3ccccc3)nc3ccccc32)n1.Cl
Reaction #79154
desired compound
Rendimiento 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccccc1/C=C/c1nc2ccccc2n1-c1ccccn1
Reaction #79161
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccc(/C=C/c2nc3ccccc3n2-c2ccccn2)c(F)c1
Reaction #79164
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2c1nc(/C=C/c1ccccc1)n2-c1ccccn1.Cl
Reaction #79193
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2c(c1)nc(/C=C/c1ccccc1)n2-c1ccccn1
Reaction #79200
(E)-5-Cyano-1-(2-pyridyl)-2-styryl-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)Oc1ccc2c(c1)nc(/C=C/c1ccccc1)n2-c1ccccn1
Reaction #79209
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #81672
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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