Substructure Search

1118079

Nc1ccc(S[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #6121
expected product
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1nn(C)c(=O)cc1Nc1ccc(SC)cc1F
Reaction #44238
desired product
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2cc(=O)n(C)nc2C(=O)NOCCO)c(F)c1
Reaction #44239
desired product
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2ncc(C#N)c2N)c(F)c1
Reaction #59657
pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)c1ccc(N2CCCC2)c(C(=O)O)c1
Reaction #60957
title compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCn1nnnc1Sc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #74876
1-(2-acetamidoethyl)-5-(2,4-dinitrophenylthio)tetrazole
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #74877
( d )
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2C=NCC2)cc1
Reaction #80598
1-[4-(methylsulfonyl)phenyl]-4,5-dihydro-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2ccnc2)cc1
Reaction #80599
1-[4-(methylsulfonyl)phenyl]-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Sc2ccc3ccccc3c2)ccc1[N+](=O)[O-]
Reaction #80907
2-nitro-5-(naphth-2-ylthio)benzonitrile
Yield 80.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Sc2ccc3ccccc3c2)ccc1N
Reaction #80908
2-amino-5-(naphth-2-ylthio)benzonitrile
Yield 103.4%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Sc2ccnc3ccccc23)cc1
Reaction #83348
4-(4-nitrophenylthio)quinoline
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Sc2ccnc3ccccc23)cc1
Reaction #83349
4-(4-aminophenylthio)quinoline
Yield 58.3%DOI: 10.6084/m9.figshare.5104873.v1
S=C(Nc1ccc(Sc2ccc3ccccc3n2)cc1)Nc1ccc(Cl)c(Cl)c1
Reaction #83371
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOCCO)ccc3[nH]ncc23)c(F)c1
Reaction #166247
solid
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(Sc2ccc(-n3cnnn3)cc2)nc(Nc2ccc(N3CCOCC3)cc2)n1
Reaction #168898
product
Yield 38.1%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC(=O)Nc1ccc(Sc2ccnc(Nc3ccc(N4CCOCC4)cc3)n2)cc1
Reaction #168903
product
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc(Sc2ccc3ccccc3c2)c(Cl)c1)c1ccc(Cl)nc1
Reaction #175076
DOI: 10.1039/C8SC04228D
COC(=O)NC(=S)Nc1ccc(SCSC)cc1[N+](=O)[O-]
Reaction #184149
DOI: 10.1039/C8SC04228D
CC(=O)Nc1cc(S(=O)c2ccccc2)ccc1[N+](=O)[O-]
Reaction #184826
DOI: 10.1039/C8SC04228D
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