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Nc1ccc(F)nc1F

O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1nc(F)ccc1[N+](=O)[O-]
Reaction #56505
title product
DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(-c2nc3ccc(F)nc3o2)cc1
Reaction #68997
[4-(5-fluoro-oxazolo[5,4-b]pyridine-2-yl)-phenyl]-methyl-amine
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #68999
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(-c2nc3ccc(F)nc3o2)cc1
Reaction #69001
[4-(5-fluoro-oxazolo[5,4-b]pyridin-2-yl)-phenyl]-dimethyl-amine
Rendimiento 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(-c3nc4ccc(F)nc4o3)cnc21
Reaction #69003
5-fluoro-2-(1-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-oxazolo[5,4-b]pyridine
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(C(=O)Nc3ccc(F)nc3F)cnc21
Reaction #69004
1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid (2,6-difluoro-pyridin-3-yl)-amide
Rendimiento 72.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2cc(-c3nc4ccc(F)nc4s3)cnc21
Reaction #69005
5-fluoro-2-(1-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-thiazolo[5,4-b]pyridine
Rendimiento 167.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1F
Reaction #163110
title compound
Rendimiento 50.5%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
O=CNc1ccc(F)nc1F
Reaction #202475
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1c(F)cc(F)nc1F
Reaction #243299
DOI: 10.1039/C8SC04228D
Nc1ccc(F)nc1F
Reaction #300869
DOI: 10.1039/C8SC04228D
CCN(c1nc(F)ccc1[N+](=O)[O-])C1CCN(Cc2ccccc2)CC1
Reaction #449035
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(c1nc(F)ccc1[N+](=O)[O-])C1CCN(Cc2ccccc2)CC1
Reaction #449041
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1F
Reaction #537565
title compound
Rendimiento 57.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nc(F)c(F)cc2[N+](=O)[O-])n[nH]1
Reaction #537566
5,6-Difluoro-N-(5-methyl-1H-pyrazol-3-yl)-3-nitropyridin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)nc1F
Reaction #633961
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CNc1ccc(F)nc1F
Reaction #633962
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CN(C=O)c1ccc(F)nc1F
Reaction #633963
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(F)nc2F)cn1
Reaction #633964
title compound
Rendimiento 95.4%DOI: 10.6084/m9.figshare.5104873.v1
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