Recherche de Sous-structure

OB(O)c1ccccc1

COC(=O)[C@H](Cc1ccccc1)n1cc(-c2cccc3ccccc23)cc(NC(=O)c2ccc(C(F)(F)F)cc2)c1=O
Reaction #7903
title compound
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cccc(-c2cccc3ccccc23)n1
Reaction #8237
2-formyl-6-naphthylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccccc2-c2ccc3c(c2)C2(c4cc(-c5ccccc5-c5ccccc5)ccc4-c4c(-c5ccccc5-c5ccccc5)cc(-c5ccccc5-c5ccccc5)cc42)c2cc(-c4ccccc4-c4ccccc4)cc(-c4ccccc4-c4ccccc4)c2-3)cc1
Reaction #8644
2,2′,4,4′,7,7′-hexabiphenylyl-9,9′-spirobifluorene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)ccc1OCC(=O)O
Reaction #9439
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(-c2cc3[nH]c4ccc(O)cc4c3c3c2C(=O)NC3=O)c1
Reaction #11114
4-(3-aminophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(C)c(-c2cccc3ccccc23)s1
Reaction #40730
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc(-c2ccnc(Cl)n2)c1
Reaction #43034
3-(2-Chloro-pyrimidin-4-yl)-benzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(B2OC(C)(C)C(C)(C)O2)cc1C(F)(F)F
Reaction #44347
4,4,5,5-tetramethyl-2-[4-(methylthio)-3-(trifluoromethyl)phenyl]-1,3,2-dioxaborolane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cc(Cl)ccc2OCc2ccccc2)cc1C(F)(F)F)N1CCCC1
Reaction #44365
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2cc(Cl)ccc2OCc2ccccc2)OC1(C)C
Reaction #44375
2-[5-chloro-2-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2cncc(-c3cccc(N)c3)n2)cc(OC)c1OC
Reaction #44530
pure title compound
Rendement 38.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nccc2scc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #45417
desired product
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)csc12)OCC
Reaction #45433
desired product
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(-c4cccc(N(C)C)c4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45454
title compound
Rendement 20.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc(N)c2)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45733
6-(3-Aminophenyl)-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(O)(O)NC1Cc2ccc(-c3cccc(S(=O)(=O)N(C)C)c3)cc2C1
Reaction #46712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(O)(O)NC1Cc2ccc(-c3cccc(S(N)(=O)=O)c3)cc2C1
Reaction #46713
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3cccc(CO)c3)c(C(=O)Nc3ccccc3)n2)cc1
Reaction #48601
4-(3-hydroxymethyl-phenyl)-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Rendement 131.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(-c3cccc(C(N)=O)c3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49490
4-(3-carbamoylphenyl)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Rendement 47.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C=C2C(=O)Nc3ccccc32)cc1-c1cccc(NC(C)=O)c1
Reaction #52665
N-[2′-methoxy-5′-(2-oxo-1,2-dihydroindol-3-ylidenemethyl)-biphenyl-3-yl]-acetamide
Rendement 22.0%DOI: 10.6084/m9.figshare.5104873.v1
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