An 21 Reaktionen beteiligt

823934

Cc1ccc2cc(C(=O)Nc3cc([N+](=O)[O-])ccc3C)ccc2n1
Reaction #465
Ausbeute 0.0%750 AstraZeneca ELN dataset
Cc1ccc([N+](=O)[O-])cc1NC1COC1
Reaction #723
Ausbeute 28.8%750 AstraZeneca ELN dataset
Cc1ccc([N+](=O)[O-])cc1-c1ccncc1Cl
Reaction #41775
3-chloro-4-(2-methyl-5-nitrophenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #69108
solid
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=Cc1ccc([N+](=O)[O-])cc1Br
Reaction #177042
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc([N+](=O)[O-])cc1Br
Reaction #179176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N)cc1Br
Reaction #197010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc([N+](=O)[O-])cc1-c1ccccc1
Reaction #207626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(N)cc1Br
Reaction #274352
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(O)c1ccc([N+](=O)[O-])cc1Br
Reaction #276585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc([N+](=O)[O-])cc1-c1cccnc1
Reaction #369212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc([N+](=O)[O-])cc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #394821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc([N+](=O)[O-])cc1-c1ccccc1
Reaction #412379
desired product
Ausbeute 57.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=C(O)c1ccc([N+](=O)[O-])cc1Br
Reaction #412387
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
Cc1ccc([N+](=O)[O-])cc1-c1ccccc1
Reaction #443267
pale orange needles
Ausbeute 57.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
O=C(O)c1ccc([N+](=O)[O-])cc1Br
Reaction #443271
2-bromo-4-nitrobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
Cc1ccc([N+](=O)[O-])cc1-c1ccccc1
Reaction #470249
desired product
Ausbeute 57.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
O=C(O)c1ccc([N+](=O)[O-])cc1Br
Reaction #470257
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
Cc1ccc(N)cc1Br
Reaction #555973
product
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(O)c1ccc([N+](=O)[O-])cc1Br
Reaction #583811
2-bromo-4-nitro-benzoic acid
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
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