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Aminophenols
Known as:
Aminophenols [Chemical/Ingredient]
, Hydroxyanilines
Phenols substituted in any position by an amino group.
National Institutes of Health
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38 relations
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2,4-diaminophenol
2,4-diaminophenol hydrochloride
2-amino-4-tert-butylphenol
2-aminophenol
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agonists
antagonists & inhibitors
aspects of radiation effects
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Can laccases catalyze bond cleavage in lignin?
Line Munk
,
A. Sitarz
,
D. Kalyani
,
J. Mikkelsen
,
A. Meyer
Biotechnology advances
2015
Corpus ID: 4927969
Highly Cited
2014
Highly Cited
2014
Pd-catalyzed chemoselective carbonylation of aminophenols with iodoarenes: alkoxycarbonylation vs aminocarbonylation.
Tongyu Xu
,
H. Alper
Journal of the American Chemical Society
2014
Corpus ID: 207114925
Palladium-catalyzed chemoselective carbonylation of aminophenols with iodoarenes was realized by changing ligand and base. 3- or…
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Highly Cited
2014
Highly Cited
2014
N-Terminal Modification of Proteins with o-Aminophenols
A. Obermeyer
,
John B. Jarman
,
M. Francis
Journal of the American Chemical Society
2014
Corpus ID: 15870277
The synthetic modification of proteins plays an important role in chemical biology and biomaterials science. These fields provide…
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Highly Cited
2012
Highly Cited
2012
Benzazoles from aliphatic amines and o-amino/mercaptan/hydroxyanilines: elemental sulfur as a highly efficient and traceless oxidizing agent.
T. Nguyen
,
L. Ermolenko
,
William A. Dean
,
A. Al‐Mourabit
Organic letters
2012
Corpus ID: 40290970
A novel remarkably simple solvent-free and catalyst-free synthesis of benzazoles from alkylamines and o-hydroxy/amino/mercaptan…
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Review
2009
Review
2009
LACCASE: PROPERTIES AND APPLICATIONS
V. Madhavi
,
S. Lele
2009
Corpus ID: 18484106
Laccases (benzenediol:oxygen oxidoreductase, EC 1.10.3.2) are multi-copper oxidases that are widely distributed among plants…
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Highly Cited
2009
Highly Cited
2009
Orthogonal Cu- and Pd-based catalyst systems for the O- and N-arylation of aminophenols.
D. Maiti
,
S. Buchwald
Journal of the American Chemical Society
2009
Corpus ID: 207149241
O- or N-arylated aminophenol products constitute a common structural motif in various potentially useful therapeutic agents and…
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Highly Cited
2008
Highly Cited
2008
Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde.
Deepak Sinha
,
A. Tiwari
,
+4 authors
A. Mishra
European journal of medicinal chemistry
2008
Corpus ID: 23709870
Highly Cited
2008
Highly Cited
2008
Application of the PM6 method to modeling the solid state
J. Stewart
Journal of molecular modeling
2008
Corpus ID: 12517322
AbstractThe applicability of the recently developed PM6 method for modeling various properties of a wide range of organic and…
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Highly Cited
2001
Highly Cited
2001
Predicting the activity of phenolic antioxidants: theoretical method, analysis of substituent effects, and application to major families of antioxidants.
J. S. Wright
,
E. Johnson
,
G. DiLabio
Journal of the American Chemical Society
2001
Corpus ID: 29613929
A procedure based on density functional theory is used for the calculation of the gas-phase bond dissociation enthalpy (BDE) and…
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Highly Cited
1957
Highly Cited
1957
Cancer of the Urinary Bladder Induced in Mice with Metabolites of Aromatic Amines and Tryptophan
M. J. Allen
,
E. Boyland
,
C. Dukes
,
E. S. Horning
,
J. Watson
British Journal of Cancer
1957
Corpus ID: 1964262
ImagesFigs. 3-5Figs. 6-8
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