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Aryl Hydrocarbon Hydroxylases

Known as: Aryl Hydrocarbon Hydroxylases [Chemical/Ingredient], microsomal p450, microsomal monooxygenase 
A large group of cytochrome P-450 (heme-thiolate) monooxygenases that complex with NAD(P)H-FLAVIN OXIDOREDUCTASE in numerous mixed-function… 
National Institutes of Health

Related topics

Related topics

49 relations

Narrower (39)

AromataseCYP19A1 protein, humanCYP1A1 protein, humanCYP2A13 protein, human
Cytochrome P-450 OxygenaseIn BloodProcess of secretionantagonists & inhibitors

Broader (2)

Cytochrome P450Oxygenases

Papers overview

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Highly Cited
2009
Highly Cited
2009
Formation of ArF from LPdAr(F): Catalytic Conversion of Aryl Triflates to Aryl Fluorides
Facile Fluorination Fluorine atoms have become a useful substituent in pharmaceuticals. However, they remain challenging to… 
Highly Cited
2006
Highly Cited
2006
A general and long-lived catalyst for the palladium-catalyzed coupling of aryl halides with thiols.
A general catalytic system for the coupling of aryl halides and sulfonates with thiols based on the use of the CyPF-t-Bu ligand… 
Highly Cited
2004
Highly Cited
2004
Sterically demanding, bioxazoline-derived N-heterocyclic carbene ligands with restricted flexibility for catalysis.
A unique family of N-heterocyclic carbenes derived from bioxazolines (IBiox) suitable for application in transition-metal… 
Highly Cited
2003
Highly Cited
2003
A general method for the Suzuki-Miyaura cross-coupling of sterically hindered aryl chlorides: synthesis of di- and tri-ortho-substituted biaryls in 2-propanol at room temperature.
The catalytic formation of di- and trisubstituted ortho biaryl junctions has been achieved using a palladacylce pre-catalyst… 
Highly Cited
2001
Highly Cited
2001
A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions.
In the presence of Cy2NMe, Pd/P(t-Bu)3 serves as an exceptionally mild and versatile catalyst for Heck reactions of aryl… 
Highly Cited
1999
Highly Cited
1999
Room-Temperature Palladium-Catalyzed Amination of Aryl Bromides and Chlorides and Extended Scope of Aromatic C-N Bond Formation with a Commercial Ligand.
The reactions of aryl bromides with amines occurs at room temperature when using Pd(0) and P(t-Bu)(3) in a 1:1 ratio, and the… 
Highly Cited
1999
Highly Cited
1999
A Highly Active Catalyst for the Room-Temperature Amination and Suzuki Coupling of Aryl Chlorides.
A unique combination of steric and electronic properties appears to determine the effectiveness of phosphanyl-substituted… 
Review
1998
Review
1998
Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and Mechanism.
  • J. Hartwig
  • Angewandte Chemie
  • 1998
  • Corpus ID: 14009917
Oxidative addition and reductive elimination are the central steps in new palladium-catalyzed chemistry that forms C-N and C-O… 
Highly Cited
1998
Highly Cited
1998
A Convenient and General Method for Pd-Catalyzed Suzuki Cross-Couplings of Aryl Chlorides and Arylboronic Acids.
From only commercially available reagents a wide array of Suzuki cross-couplings of aryl chlorides with arylboronic acids can be… 
Highly Cited
1995
Highly Cited
1995
Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents
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