Поиск подструктуры

1433915

N#Cc1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)c1
Reaction #2842
title compound
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CCN(Cc2cccc(C#N)c2)C1=O)S(=O)(=O)c1cc2ccccc2s1
Reaction #2843
title compound
Выход 96.7%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CC[C@H](NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2848
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(O)c(CN2CCC(NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #2855
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(CN2CC[C@H](NS(=O)(=O)c3cc4ccccc4s3)C2=O)ccc1N
Reaction #2866
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(O)c(CN2CC[C@H](NS(=O)(=O)c3cc4ccc(Cl)cc4s3)C2=O)c1
Reaction #2873
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8424
hydrochloride salt
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3cc4ccccc4s3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49435
4-(benzothiophene-2-sulfonyloxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(S(=O)(=O)c2ccc(=O)[nH]n2)sc2ccc(Cl)cc12
Reaction #51019
6-(5-Chloro-3-methyl-benzothiophene-2-sulfonyl)-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1(CCc2ccccc2CO)CC(O)=C(Sc2sc3ccccc3c2C(C)(C)C)C(=O)O1
Reaction #51791
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2c(C)cc(C)nc2n1-c1ccc(CCNC(=O)NS(=O)(=O)c2cc3ccccc3s2)cc1
Reaction #78709
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CCN(c3cc4ccccc4s3)CC2)cc1
Reaction #82494
title compound
Выход 46.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(NS(=O)(=O)c2cc3ccc(F)cc3s2)CCN1Cc1cc2ncccc2o1
Reaction #177024
DOI: 10.1039/C8SC04228D
COc1ccc(C(F)(F)F)cc1S(=O)(=O)Nc1ccccc1NS(=O)(=O)c1cc2ccccc2s1
Reaction #186672
DOI: 10.1039/C8SC04228D
Cc1c(SCC(=O)N2CCCc3ccccc32)sc2ccccc12
Reaction #187576
DOI: 10.1039/C8SC04228D
CN(C)CCS(=O)Cc1ccc2sc(S(N)(=O)=O)cc2c1
Reaction #188711
DOI: 10.1039/C8SC04228D
N=C(NC(=O)OCC(Cl)(Cl)Cl)c1cccc(CN2CCC(NS(=O)(=O)c3cc4c(Cl)cc(Cl)cc4s3)C2=O)c1
Reaction #191311
DOI: 10.1039/C8SC04228D
Cc1c(S(=O)(=O)c2ccc(=O)[nH]n2)sc2ccc(Cl)cc12
Reaction #196269
DOI: 10.1039/C8SC04228D
Cl
Reaction #199968
DOI: 10.1039/C8SC04228D
CCCc1cc(SCCN(CCC)S(=O)(=O)c2sc3ccc(Cl)cc3c2C)ccc1OCC(=O)OCC
Reaction #204041
DOI: 10.1039/C8SC04228D
Страница 1Далее