Busqueda de Subestructura

151063

COc1ccc(Cl)c(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1.[Br-]
Reaction #11182
phosphonium
Rendimiento 76.0%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
CC(=O)N1C[C@H]2CC(c3ccc(OCCOc4cc(F)ccc4Cl)cc3)=C(C(=O)N(Cc3cc4c(cc3Cl)OCO4)C3CC3)[C@@H](C1)N2.O=CO
Reaction #61354
(rac.)-(1R*,5S*)-3-Acetyl-7-{4-[2-(2-chloro-5-fluorophenoxy)ethoxy]phenyl}-3,9-diazabicyclo[3.3.1]non-6-ene-6-carboxylic acid (6-chlorobenzo[1,3]-dioxol-5-ylmethyl)cyclopropylamide formate salt
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(Cl)c(CN2CCCCC2)c1
Reaction #63873
N-(2-chloro-5-hydroxybenzyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ncc[nH]3)c3nccnc23)c1Cl
Reaction #71337
title compound
Rendimiento 79.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3nccn3COCC[Si](C)(C)C)c3nccnc23)c1Cl
Reaction #71338
title compound
Rendimiento 85.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2cnc3c(-c4c(Cl)c(OC)cc(OC)c4Cl)ccc(C(=O)Nc4cccnc4)c3n2)CC1
Reaction #71381
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2cnc3c(-c4c(Cl)c(OC)cc(OC)c4Cl)ccc(C(=O)O)c3n2)CC1
Reaction #71382
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2cnc3c(C(=O)Nc4cccnc4)ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c3n2)CC1
Reaction #71384
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2cnc3c(C(=O)Nc4ccccn4)ccc(-c4c(Cl)c(OC)cc(OC)c4Cl)c3n2)CC1
Reaction #71385
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)O)c3ncc(N(C)CCN(C)C)nc23)c1Cl
Reaction #71386
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccccn3)c3ncc(N(C)CCN(C)C)nc23)c1Cl
Reaction #71390
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)cn3)c3nc(C)c(C)nc23)c1Cl
Reaction #71437
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCN(C)CC4)cn3)c3nccnc23)c1F
Reaction #71456
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2c(F)c(OC)cc(OC)c2Cl)c2nccnc12
Reaction #71457
title compound
Rendimiento 82.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4c(F)c(OC)cc(OC)c4Cl)c4nccnc34)nc2)CC1
Reaction #71458
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN4CCNC(=O)C4)cn3)c3nccnc23)c1F
Reaction #71459
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN(C)CCN(C)C)cn3)c3nccnc23)c1F
Reaction #71460
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN(C)CC(=O)N(C)C)cn3)c3nccnc23)c1F
Reaction #71461
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3ccc(CN(C)CC(N)=O)cn3)c3nccnc23)c1F
Reaction #71462
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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