Substructure Search

O=S=O

CS(=O)(=O)Nc1cccc2c(C3(CCCN4CCOCC4)CCc4cc(F)ccc43)c[nH]c12
Reaction #41998
title compound
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OS(N)(=O)=O)CC[C@@H]1[C@@H]2CC[C@]2(C)/C(=N/O)CC[C@@H]12
Reaction #60577
2-methoxy-(E)-17-(oximino)-estra-1,3,5(10)-trien-3-yl sulfamate
Yield 74.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)NS(=O)(=O)c2ccc(Cl)s2)cc1
Reaction #66419
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NS(=O)(=O)c1ccc(Cl)s1)c1ccc(N2C(=O)c3ccccc3C2=O)cc1
Reaction #66420
desired compound
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)N[C@@H]1Cc2ccc(Br)cc2C1
Reaction #71260
(R)—N-(5-bromo-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamide
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)[C@H]2CC[C@]1(CS(=O)(=O)O)C(=O)C2.N[C@H]1Cc2ccc(Br)cc2C1
Reaction #71264
fluffy white solid
Yield 37.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1Cc2ccc(Br)cc2C1)OCc1ccccc1
Reaction #71268
(R)-benzyl 5-bromo-2,3-dihydro-1H-inden-2-ylcarbamate
Yield 89.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccc(Br)cc2C1)OCc1ccccc1
Reaction #71273
(S)-benzyl 5-bromo-2,3-dihydro-1H-inden-2-ylcarbamate
Yield 108.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2cn(C)cn2)cc1
Reaction #78730
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(C(F)(F)F)c(Cl)cc2n1-c1ccc(CCOC(=O)NS(=O)(=O)c2cn(C)c(C)n2)cc1
Reaction #78731
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(OCCNS(C)(=O)=O)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89999
compound
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(OS(=O)(=O)C(F)(F)F)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90009
Trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCN(c2ccc3c(c2)C(C)(C)c2[nH]c4cc(C#N)ccc4c2C3=O)CC1
Reaction #90010
8-(4-Isopropyl-piperazin-1-yl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCN(CCO)CC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCOCC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90012
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCC(N4CCCC4)CC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90013
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc3c(c2)C(C)(C)c2[nH]c4cc(C#N)ccc4c2C3=O)CC1
Reaction #90014
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCCCC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90015
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCC(O)CC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90016
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCN(S(C)(=O)=O)CC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90018
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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