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1242446

CN1C(=O)C(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)SC1=S
Reaction #3035
title compound
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3036
title compound
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3039
desired titled compound
Выход 59.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)N1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3042
desired product
Выход 29.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)N1C(=O)C(=CCc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)SC1=S
Reaction #3044
5-[[3,5-bis(1,1-dimethylethyl) -4-hydroxyphenyl]methylmethylene]-3-(dimethylamino)-2-thioxo-4-thiazolidinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(SC(=S)N(C)C)c1ccccc1)[N+](=O)[O-]
Reaction #54418
α-(1-nitroethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=S)SC(C[N+](=O)[O-])c1ccccc1
Reaction #54419
α-(nitromethyl)benzyl diethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(C[N+](=O)[O-])SC(=S)N(C)C)c1OC(C)=O
Reaction #54420
2-acetoxy-3-methoxy-α-(nitromethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(C(C[N+](=O)[O-])SC(=S)N(C)C)cc1
Reaction #54423
4-acetoxy-α-(nitromethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)N1CCSC1=Nc1ccccc1C(C)C
Reaction #57301
2-(2-isopropylphenyl)imino-3-(methylthio)thiocarbonyl-1,3-thiazolidine
Выход 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)N1[C@@H](CO)Cc2c([nH]c3ccccc23)[C@@H]1C
Reaction #93333
Methyl (1RS, 3SR)-trans-3-hydroxymethyl-1-methyl-1,2,3,4-tetrahydro-β-carboline-2-carbodithioate
DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)N1[C@H](CO)Cc2c([nH]c3ccccc23)[C@@H]1C1CCCCC1
Reaction #93341
title compound
Выход 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)N1[C@H](CO)Cc2c([nH]c3ccccc23)[C@@H]1c1ccccc1
Reaction #93342
title compound
Выход 78.1%DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1ccc(CSC(=S)N2Cc3[nH]c4ccccc4c3C[C@H]2CO)cc1
Reaction #93347
title compound
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(CSC(=S)N2Cc3[nH]c4ccccc4c3CC2CO)cc1
Reaction #93348
4-Nitrobenzyl (3RS)-3-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline-2-carbodithioate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC(=S)N2Cc3[nH]c4ccccc4c3CC2CO)cc1
Reaction #93349
title compound
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(S)=Cc1ccc(C(F)(F)F)o1
Reaction #94394
α-mercapto-β-(5-trifluoromethyl-2-furyl)acrylic acid
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(S)=Cc1ccc(C(F)(F)F)o1
Reaction #96199
α-mercapto-β-(5-trifluoromethyl-2-furyl)acrylic acid
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc2ccc(C=C3SC(=S)NC3=O)cc2c1-c1cccnc1
Reaction #174877
DOI: 10.1039/C8SC04228D
O=C1C(=Cc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #175164
DOI: 10.1039/C8SC04228D
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