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3612

CCOC(=O)c1cnc(Nc2ccc([N+](=O)[O-])cn2)o1
Reaction #586
Выход 85.6%
O=[N+]([O-])c1ccc(F)nc1
Reaction #3393
2-Fluoro-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc([N+](=O)[O-])cnc1F
Reaction #3411
title compound
Выход 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)cnc1Cl
Reaction #3415
solid
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
NNc1ccc([N+](=O)[O-])cn1
Reaction #8152
(5-nitropyridin-2-yl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cl)[nH]c(=O)c([N+](=O)[O-])c1O
Reaction #11466
6-chloro-4-hydroxy-5-methyl-3-nitro-1H-pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc([N+](=O)[O-])cn1
Reaction #41784
2-(dimethylamino)-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCNc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #42790
N-(2-(6-chloro-3-nitropyridin-2-ylamino)ethyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #48365
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)Nc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #49806
compound A
Выход 69.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1Nc2nc(Cl)ccc2NC1=O
Reaction #49807
pure product
Выход 24.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Nc2nc(Cl)ccc2NC1=O
Reaction #49811
compound
Выход 61.2%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N2CCSCC2)nc1
Reaction #50920
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@H](Nc2ccc([N+](=O)[O-])cn2)CC1
Reaction #51215
N-(5-nitro-2-pyridyl)-trans-1,4-cyclohexanediamine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(N[C@H]2CC[C@H](O)CC2)nc1
Reaction #51219
trans-4-(5-nitro-2-pyridylamino)cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@H](Oc2ccc([N+](=O)[O-])cn2)CC1
Reaction #51220
trans-1-tert-butoxycarbonylamino-4-(5-nitro-2-pyridyloxy)cyclohexane
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Sc2ccccc2)ccc1[N+](=O)[O-]
Reaction #52205
2-amino-3-nitro-6-(phenylmercapto)pyridine
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #54141
yellow solid
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
NNc1ccc([N+](=O)[O-])cn1
Reaction #54148
2-Hydrazino-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc3c(c2)CCC(c2ccccc2)O3)nc1
Reaction #59444
5-Nitro-2-(2-phenylchroman-6-yloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
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