4-tert-butyl-2-nitroaniline

Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #165486
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #578249
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CC(C)(C)c1cc(Br)c(N)c([N+](=O)[O-])c1
Reaction #595503
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #685616
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CC(C)(C)c1ccc(NC(=O)CCC2CC(=O)C2)c([N+](=O)[O-])c1
Reaction #794845
N-(4-tert-butyl-2-nitrophenyl)-3-(3-oxo-cyclobutyl)propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(C)(C)c1ccc(NC(=O)CCC2CC(=O)C2)c([N+](=O)[O-])c1
Reaction #794848
N-(4-tert-butyl-2-nitrophenyl)-3-(3-oxo-cyclobutyl)propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(C)(C)c1ccc(NC(=O)CCC2CC(=O)C2)c([N+](=O)[O-])c1
Reaction #794849
N-(4-tert-butyl-2-nitrophenyl)-3-(3-oxo-cyclobutyl)propanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(C)(C)c1ccc(NC(=O)CCC2CC(=O)C2)c([N+](=O)[O-])c1
Reaction #794854
12
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #986125
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CC(C)(C)c1ccc(NC(=O)c2ccc(Cl)nc2)c([N+](=O)[O-])c1
Reaction #1094396
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
CC(C)(C)c1ccc(NCc2ccccc2)c([N+](=O)[O-])c1
Reaction #1511419
title compound
Ausbeute 63.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_01
CC(C)(C)c1ccc(NC(=O)c2ccc(Cl)nc2)c([N+](=O)[O-])c1
Reaction #1631488
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #1732246
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #1855460
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06
CC(C)(C)c1cc(Br)c(N)c([N+](=O)[O-])c1
Reaction #1973966
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
CC(C)(C)c1cc(Br)c(N)c([N+](=O)[O-])c1
Reaction #2017443
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
CC(C)(C)c1cc(Br)c(N)c([N+](=O)[O-])c1
Reaction #2049482
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
Cc1ccc(C)n1-c1ccc(C(C)(C)C)cc1[N+](=O)[O-]
Reaction #2165728
1-(4-tert-butyl-2-nitrophenyl)-2,5-dimethylpyrrole
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_04
CC(C)(C)c1cc(Br)c(N)c([N+](=O)[O-])c1
Reaction #2367780
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
CC(C)(C)c1cc(Br)c(N)c([N+](=O)[O-])c1
Reaction #2447190
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04