Busqueda de Subestructura

C=Cc1ccccc1Cl

CCc1nccc(NC2CCC(=Cc3ccc(Cl)cc3Cl)CC2)c1Cl
Reaction #1116
3-Chloro-4-[4-(2,4-dichlorobenzylidene)cyclohexyl]amino-2-ethylpyridine
Rendimiento 7.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccc2Cl)N2CCC1CC2
Reaction #5074
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1Cl
Reaction #5075
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC=C(C#N)c1ccc(C(F)(F)F)cc1Cl
Reaction #10174
4-(2-chloro-4-trifluoromethyl-phenyl)-4-cyano-but-3-enoic acid methyl ester
Rendimiento 97.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)cc(C=Cc1c(Cl)cccc1OC)n2CCO
Reaction #11149
2-{2-[2-(2-Chloro-6-methoxyphenyl)ethenyl]-5-methoxy-1H-indol-1-yl}ethanol
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(/C=C/c3c(Cl)cccc3Cl)cc2c1
Reaction #11163
2-[(E)-2-(2,6-Dichlorophenyl)ethenyl]-5-methoxy-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C/c2cc3cc(OC)ccc3[nH]2)c(Cl)c1
Reaction #11181
2-[(E)-2-(2-Chloro-4-methoxyphenyl)ethenyl]-5-methoxy-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)c(/C=C/c2cc3cc(OC)ccc3[nH]2)c1
Reaction #11183
2-[(E)-2-(2-Chloro-5-methoxyphenyl)ethenyl]-5-methoxy-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c(c1Cl)CNC2=O
Reaction #49588
4-chloro-5-vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1cc(NN)ccc1Cl
Reaction #76775
ethyl 2-chloro-5-hydrazinocinnamate
Rendimiento 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC=C(C)c1cc(Cl)ccc1Cl)C(C)=O
Reaction #82520
ethyl 2-methylcarbonyl-5-(2,5-dichlorophenyl)-4-hexenoate
Rendimiento 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=CCc1c(C)nc(N)nc1O)c1cc(Cl)ccc1Cl
Reaction #82521
2-amino-4-hydroxy-6-methyl-5-[3-(2,5-dichlorophenyl)-2-butenyl]pyrimidine
Rendimiento 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCSC1(C(O)(C=Cc2ccc(Cl)cc2Cl)Cn2cncn2)CC1
Reaction #176119
DOI: 10.1039/C8SC04228D
CC(C)(C)C(O)C(=Cc1ccc(Cl)cc1Cl)n1cncn1
Reaction #181547
DOI: 10.1039/C8SC04228D
CC(C)C(=O)OC1=C(c2c(F)ccc(Br)c2Cl)S(=O)(=O)Cc2nccnc21
Reaction #191275
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)C(C#N)=Cc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)c(F)cc1Cl
Reaction #193066
DOI: 10.1039/C8SC04228D
Cc1nnc2n1-c1ccc(N)cc1C(c1ccccc1Cl)=CC2
Reaction #196727
DOI: 10.1039/C8SC04228D
CCCCC(Oc1ccc(C=CC(=O)OCC)c(Cl)c1)c1cccc(-c2ccc(C(F)(F)F)cc2)n1
Reaction #210041
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCC(O)Cc1cccc(C=Cc2c(Cl)cccc2Cl)c1
Reaction #210737
DOI: 10.1039/C8SC04228D
CC(=Cc1ccc(Cl)cc1Cl)[N+](=O)[O-]
Reaction #212269
DOI: 10.1039/C8SC04228D
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