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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=[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
O=[N+]([O-])c1cc(F)c(F)nc1NC(CO)c1ccc(F)cc1
Reaction #890586
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(F)c(F)nc1F
Reaction #897663
DOI: 10.1039/C8SC04228D
CC(Nc1nc(F)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #1222378
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(F)c(F)nc1F
Reaction #1321628
DOI: 10.1039/C8SC04228D
C[C@H](Nc1nc(F)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #1524619
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1F
Reaction #1524620
title compound
Rendimiento 50.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nc(F)c(F)cc2[N+](=O)[O-])n[nH]1
Reaction #1647124
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(F)c(F)nc1F
Reaction #2277070
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 #2277071
title compound
Rendimiento 57.2%DOI: 10.6084/m9.figshare.5104873.v1