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Cc1ccc(I)cc1C

Cc1ccc(N(c2ccc(-c3ccccc3)cc2)c2ccc(C)c(C)c2)cc1C
Reaction #1397
above product
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(I)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(-c2cccnc2)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(C#N)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45323
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(I)cc2C1
Reaction #46696
title compound
Выход 437.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc([N+](=O)[O-])c3)cc2C1
Reaction #46697
oil
Выход 109.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(-c2ccc3c(c2)CC(NS(=O)(=O)C(C)C)C3)c1
Reaction #46701
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(C#N)c3)cc2C1
Reaction #46705
title compound
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
CCc1ccc(I)c2c1CNC2=O
Reaction #49466
7-iodo-4-ethylisoindolinone
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2cccc(I)c21
Reaction #49468
7-iodoisoindolinone
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cccc3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49469
7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(Br)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21
Reaction #60235
yellow solid
Выход 69.9%DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(C)(O)c1cc2cc(C#N)c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61221
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-n2nccn2)cc1C=O
Reaction #69875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(C)(O)c1cc2cc(C#N)c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #84238
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cc(C(F)(F)F)c(C#N)cc1I
Reaction #84241
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1I)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90155
title compound
Выход 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1N1CCC(O)CC1)C(C)(C)c1[nH]c3cc(C#N)ccc3c1C2=O
Reaction #90158
9-Ethyl-8-(4-hydroxy-piperidin-1-yl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
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