3-hydroxy-2-nitropyridine

O=[N+]([O-])c1nc(Br)ccc1O
Reaction #398176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=[N+]([O-])c1ncccc1OCc1c(Cl)ccc(F)c1Cl
Reaction #513091
3-(2,6-dichloro-3-fluoro-benzyloxy)-2-nitro-pyridine
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1cccnc1[N+](=O)[O-]
Reaction #616353
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cccnc1[N+](=O)[O-]
Reaction #643691
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CC(Oc1cccnc1[N+](=O)[O-])c1c(Cl)ccc(F)c1Cl
Reaction #674289
(±)-3-(1-(2,6,-dichloro-3-fluorophenyl)ethoxy)-2-nitropyridine
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=[N+]([O-])c1nc(Br)ccc1O
Reaction #726222
material
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=[N+]([O-])c1nc(Br)ccc1O
Reaction #726234
material
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=[N+]([O-])c1nc(Br)ccc1O
Reaction #726240
material
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
O=[N+]([O-])c1nc(Br)ccc1O
Reaction #810706
material
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
O=[N+]([O-])c1nc(Br)ccc1O
Reaction #821400
material
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CC(Oc1cccnc1[N+](=O)[O-])c1c(Cl)ccc(F)c1Cl
Reaction #888952
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=Cc1ccc2c(n1)NC(=O)CO2
Reaction #972857
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COC(=O)C(C)(C)COc1cccnc1[N+](=O)[O-]
Reaction #1027223
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1ccc(OCc2ccc(Cl)cc2)cn1
Reaction #1048140
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=[N+]([O-])c1nc(Br)ccc1O
Reaction #1057564
material
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
CCOC(=O)CCCOc1cccnc1[N+](=O)[O-]
Reaction #1090429
product ( 40 )
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_04
COc1cccnc1[N+](=O)[O-]
Reaction #1115127
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COc1cccnc1[N+](=O)[O-]
Reaction #1234283
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=[N+]([O-])c1ncccc1OCc1c(Cl)ccc(F)c1Cl
Reaction #1256883
3-(2,6-dichloro-3-fluoro-benzyloxy)-2-nitro-pyridine
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
O=Cc1ccc2c(n1)NC(=O)CO2
Reaction #1263869
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
Seite 1Weiter