Recherche de Sous-structure

O=CO

CC(C)(C)OCC(NC(=O)c1ccccc1SSc1ccccc1C(=O)NC(COC(C)(C)C)C(=O)O)C(=O)O
Reaction #3805
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(C2CCCCC2)c2nc(SC)ncc2C1=O
Reaction #40627
title compound
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C2CCCCC2)c2nc(SC)ncc2c1=O
Reaction #40628
title compound
Rendement 102.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(Br)cc1Cl
Reaction #52990
4-bromo-2,6-dichlorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(O)cc1Cl
Reaction #52991
2,6-dichloro-4-hydroxybenzoic acid methyl ester
Rendement 54.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(Cl)cc(-c2ccccc2)cc1Cl
Reaction #52998
2,6-dichloro-4-phenylbenzoic acid methyl ester
Rendement 104.7%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #53414
83
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CBr)c(Cl)c1Cl
Reaction #65279
material
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccccn2)cc1
Reaction #78723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2ccncc2)cc1
Reaction #78724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(C[C@@H](C)OC(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #78726
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2cccc3cnccc23)cc1
Reaction #78729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2ccccc2)Nc2c(C(=O)O)cnn21
Reaction #92037
title compound
Rendement 83.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccc(NS(=O)(=O)c2ccc3c(S(=O)(=O)Nc4ccc(C(=O)[O-])cc4)cc(S(=O)(=O)Nc4ccc(C(=O)[O-])cc4)cc3c2)cc1.[Na+].[Na+].[Na+]
Reaction #94502
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@@H]1CCCN1C(=O)Oc1cc(F)c(C=O)c(F)c1
Reaction #155433
(S)-3,5-difluoro-4-formylphenyl 2-(acetoxymethyl)pyrrolidine-1-carboxylate
Rendement 50.1%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc2cc(CNS(=O)(=O)c3ccc(C(=O)OC)cc3)ccc2n1
Reaction #160262
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc2cc(CN(c3ncc(C(F)(F)F)cc3Cl)S(=O)(=O)c3ccc(C(=O)OC)cc3)ccc2n1
Reaction #160263
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c(C(=O)O)nc1Cl
Reaction #164687
3,5-Diamino-6-chloropyrazine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N=C(NCCc1ccc(N)cc1)N1C(N)=C(Cl)N=C(C(N)=O)C1N
Reaction #168495
83
Rendement 11.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)c2cnc(SCc3c(F)cc(S(=O)(=O)N(CCC[N+](C)(C)C)Cc4ccc(C(=O)O)cc4)cc3F)n2-c2ccc(F)cc2)ccc1Cl.[Cl-]
Reaction #171017
title product
Rendement 187.8%DOI: 10.6084/m9.figshare.5104873.v1
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