Skip to search formSkip to main contentSkip to account menu

Aminophenols

Known as: Aminophenols [Chemical/Ingredient], Hydroxyanilines 
Phenols substituted in any position by an amino group.
National Institutes of Health

Related topics

Related topics

38 relations

Narrower (32)

2,4-diaminophenol2,4-diaminophenol hydrochloride2-amino-4-tert-butylphenol2-aminophenol
In Bloodagonistsantagonists & inhibitorsaspects of radiation effects

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Can laccases catalyze bond cleavage in lignin?
Highly Cited
2014
Highly Cited
2014
Pd-catalyzed chemoselective carbonylation of aminophenols with iodoarenes: alkoxycarbonylation vs aminocarbonylation.
Palladium-catalyzed chemoselective carbonylation of aminophenols with iodoarenes was realized by changing ligand and base. 3- or… 
Highly Cited
2014
Highly Cited
2014
N-Terminal Modification of Proteins with o-Aminophenols
The synthetic modification of proteins plays an important role in chemical biology and biomaterials science. These fields provide… 
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.
A novel remarkably simple solvent-free and catalyst-free synthesis of benzazoles from alkylamines and o-hydroxy/amino/mercaptan… 
Review
2009
Review
2009
LACCASE: PROPERTIES AND APPLICATIONS
Laccases (benzenediol:oxygen oxidoreductase, EC 1.10.3.2) are multi-copper oxidases that are widely distributed among plants… 
Highly Cited
2009
Highly Cited
2009
Orthogonal Cu- and Pd-based catalyst systems for the O- and N-arylation of aminophenols.
O- or N-arylated aminophenol products constitute a common structural motif in various potentially useful therapeutic agents and… 
Highly Cited
2008
Highly Cited
2008
Synthesis, characterization and biological activity of Schiff base analogues of indole-3-carboxaldehyde.
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… 
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.
A procedure based on density functional theory is used for the calculation of the gas-phase bond dissociation enthalpy (BDE) and… 
Highly Cited
1957
Highly Cited
1957
Cancer of the Urinary Bladder Induced in Mice with Metabolites of Aromatic Amines and Tryptophan
ImagesFigs. 3-5Figs. 6-8 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License