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48957

CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C(N)=S)OCO3
Reaction #53335
title compound
収率 76.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C(=S)NN)OCO3
Reaction #53336
crude product
収率 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)NNC(=S)N1N=C(c2ccc([N+](=O)[O-])cc2)c2cc3c(cc2CC1C)OCO3
Reaction #53340
(±)-1-{8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbothioyl}-4-methyl-semicarbazide
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nccs1)OCO3
Reaction #53341
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53342
title compound
収率 82.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)s1
Reaction #53343
title compound
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)sc1C
Reaction #53344
title compound
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53345
title compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NC(=O)CS1)OCO3
Reaction #53346
title compound
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1SC(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)=NC1=O
Reaction #53347
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NC(=O)CCS1)OCO3
Reaction #53348
title compound
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nncs1)OCO3
Reaction #53350
title compound
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)s1
Reaction #53351
title compound
収率 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NNC(=S)N1N=C(c2ccc([N+](=O)[O-])cc2)c2cc3c(cc2C[C@H]1C)OCO3
Reaction #53352
(R)—N′-{8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbothioyl}-acetic hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
CC1=NN=C(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)SC1
Reaction #53354
title compound
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1C1=NNC(=O)CS1)OCO3
Reaction #53355
title compound
収率 37.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1n[nH]c(=O)s1)OCO3
Reaction #53356
title compound
収率 70.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3C[C@H]2C)OCO4)o1
Reaction #53357
title compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nc(=O)n(C)s1)OCO3
Reaction #53358
title compound
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)NNC(=S)N1N=C(c2ccc([N+](=O)[O-])cc2)c2cc3c(cc2CC1C)OCO3
Reaction #760392
DOI: 10.1039/C8SC04228D
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