Recherche de Sous-structure

C1CC1

Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41036
title compound
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41037
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52392
oil
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2cc(C3CC3)c3c(c2)C(C)(C)CC2(CC2)O3)cc1F
Reaction #52393
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52395
solid
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=c2ccoc2=NCN1c1ccc(NC(=O)C2(c3ccccc3)CC2)cc1
Reaction #60783
4-Amino-3-(4-((1-phenylcyclopropanecarbonyl)amino)-phenyl)furo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1cccc2ccc(OC3C=CCCC3)cc12)C1CCC1
Reaction #65567
N-{2-[7-(cyclohexen-3-yl)oxy-1-naphthyl]ethyl}cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(-c2ccccc2Cl)nc1
Reaction #70339
expected product
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(-c2ccccc2C2CC2)nc1
Reaction #70340
5-Cyclopropyl-2-(2-(2-cyclopropylphenyl)pyrimidin-5-ylamino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79961
oil
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1ccc(C#Cc2cc(C3CC3)c3c(c2)C(C)(C)CC2(CC2)O3)cc1F
Reaction #79962
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79964
solid
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1cccc2ccc(OC3C=CCCC3)cc12)C1CCC1
Reaction #80570
N-{2-[7-(cyclohexen-3-yl)oxy-1-naphthyl]ethyl}cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(C2CC2C(=O)O)cc1F
Reaction #91239
title compound
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1ncccc1COc1ccc(C2CC2C(=O)O)cc1Cl
Reaction #91250
title compound
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncccc1COc1ccc(C2CC2C(=O)O)cc1F
Reaction #91268
title compound
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1ncccc1COc1ccc(C2CC2CC(=O)O)cc1F
Reaction #91270
title compound
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccc(OCc2cccnc2SCC2CC2)c(F)c1
Reaction #91286
title compound
Rendement 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1ccc(OCc2cccnc2SCC2CC2)c(Cl)c1
Reaction #91293
title compound
Rendement 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c1cccc(C=C(Br)Br)c1
Reaction #93196
3-(2,2-Dibromovinyl)-α-cyanobenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant