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Nc1cc(F)cnc1N

CCOC(=O)CNc1ncc(F)cc1N
Reaction #562
収率 0.0%
—
Reaction #48371
EtOAc hexanes
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=Nc1cc(F)cnc1N
Reaction #48372
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(F)cnc1N
Reaction #48373
title compound
収率 92.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(n2c(=O)[nH]c3ncc(F)cc32)CC1
Reaction #48374
title compound
収率 39.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #163069
title compound
収率 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #163070
title compound
収率 40.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(C(C)Nc2nc(Nc3cc(C4CC4)[nH]n3)c(F)cc2C#N)ccc1F
Reaction #163096
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1N[C@H](CO)c1ccc(F)cc1
Reaction #163111
(S)-2-(5,6-Difluoro-3-nitropyridin-2-ylamino)-2-(4-fluorophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(F)cnc1Nc1ccc(OCc2ccccc2)cc1
Reaction #169853
title compound
収率 24.3%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(-c2ccc(O)cc2)c2ncc(F)cc21
Reaction #169854
title compound
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(F)cnc1Nc1ccc(OCc2ccccc2)cc1
Reaction #169856
title compound
収率 24.3%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(-c2ccc(O)cc2)c2ncc(F)cc21
Reaction #169857
title compound
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(F)cc1[N+](=O)[O-]
Reaction #177791
DOI: 10.1039/C8SC04228D
CC(C)(C)C(=O)Nc1ncc(F)cc1N=[N+]=[N-]
Reaction #253612
DOI: 10.1039/C8SC04228D
Nc1cc(F)cnc1N
Reaction #270528
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(F)cnc1N1CCc2ccccc2C1
Reaction #295665
DOI: 10.1039/C8SC04228D
—
Reaction #359071
EtOAc hexanes
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=Nc1cc(F)cnc1N
Reaction #359072
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(F)cnc1N
Reaction #359073
title compound
収率 92.8%DOI: 10.6084/m9.figshare.5104873.v1
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