Busqueda de Subestructura

CSC

NC1C(=O)N2C(C(=O)O)=C(OCc3ccccc3)CS[C@H]12
Reaction #5257
3-benzyloxy-7-amino-ceph-3-eme-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCS(C)(=O)=O)cc(C)c1-c1cccc(CO)c1
Reaction #43915
title compound
Rendimiento 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOc1cc(C)c(-c2cccc(CO)c2)c(C)c1
Reaction #43917
title compound
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOc1cc(C)c(-c2cccc(COc3ccc4c(c3)OC[C@H]4CC(=O)OC)c2)c(C)c1
Reaction #43918
title compound
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCS(C)(=O)=O)c(F)c(C)c1-c1cccc(CO)c1
Reaction #43922
title compound
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4C)c3)ccc21
Reaction #43948
title compound
Rendimiento 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)c(F)c4C)c3)ccc21
Reaction #43951
title compound
Rendimiento 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCOCc1cc(C(=O)NOCCO)c(Nc2ccc(I)cc2F)c(F)c1F
Reaction #49035
3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methanesulfonyl-ethoxymethyl)-benzamide
Rendimiento 21.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC2(C(=O)O)Cc3ccccc3C2)cc1
Reaction #50786
2-carboxy-2-(4-methoxybenzylthio)indan
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)NCc1ccc(-c2ccccc2C(=O)OC(C)(C)C)cc1
Reaction #64449
Methyl N-[[2'-(t-Butoxycarbonyl)biphenyl-4-yl]methyl]dithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC2(C(=O)O)Cc3ccccc3C2)cc1
Reaction #65653
2-carboxy-2-(4-methoxybenzylthio)indan
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1n[nH]c2c1CCc1cnc(SC)nc1-2
Reaction #74072
title compound
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSC(=S)c1cccc(Cl)c1CCc1cc(Br)ccc1OC
Reaction #75566
orange powder
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Br)cc1CCc1c(Cl)cccc1C1=NC2CCCCC2N1
Reaction #75567
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCSC1=Nc2ccc(C#Cc3ccc(C(=O)OCC)cc3)cc2C(C)(C)C1
Reaction #80718
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSC1=Nc2ccc(C#Cc3ccc(C(=O)O)cc3)cc2C(C)(C)C1
Reaction #80720
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCSC1=Nc2ccc(C#Cc3ccc(C(=O)O)cc3)cc2C(C)(C)C1
Reaction #80721
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(C(=O)SCC2C(=O)OCC2c2ccccc2)cc1
Reaction #93538
title compound
Rendimiento 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccc(Cl)cc1)c1ccccc1
Reaction #93539
title compound
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(SCC1C(=O)OCC1c1ccccc1)c1ccccc1F
Reaction #93540
title compound
Rendimiento 67.2%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente