Related references
Note: Only part of the references are listed.Synthesis of Aryl Trimethylstannanes from Aryl Amines: A Sandmeyer-Type Stannylation Reaction
Di Qiu et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)
Synthesis of Pinacol Arylboronates from Aromatic Amines: A Metal-Free Transformation
Di Qiu et al.
JOURNAL OF ORGANIC CHEMISTRY (2013)
C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
Joanna Wencel-Delord et al.
NATURE CHEMISTRY (2013)
Recent advances in transition-metal-free direct C-C and C-heteroatom bond forming reactions
Vaibhav P. Mehta et al.
RSC ADVANCES (2013)
Transition-Metal-Free Direct Arylation of Anilines
Tracey Pirali et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2012)
Base- and metal-free C-H direct arylations of naphthalene and other unbiased arenes with diaryliodonium salts
Susana Castro et al.
CHEMICAL COMMUNICATIONS (2012)
Transition-Metal-Free Oxyarylation of Alkenes with Aryl Diazonium Salts and TEMPONa
Marcel Hartmann et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)
Metal-Free, Visible-Light-Mediated Direct C-H Arylation of Heteroarenes with Aryl Diazonium Salts
Durga Prasad Hari et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)
Direct Intermolecular Aniline Ortho-Arylation via Benzyne Intermediates
Thanh Truong et al.
ORGANIC LETTERS (2012)
Visible Light Photocatalytic Synthesis of Benzothiophenes
Durga Prasad Hari et al.
ORGANIC LETTERS (2012)
Organocatalysis and C-H Activation Meet Radical- and Electron-Transfer Reactions
Armido Studer et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2011)
Metal-Free Direct Arylations of Indoles and Pyrroles with Diaryliodonium Salts
Lutz Ackermann et al.
ORGANIC LETTERS (2011)
Direct Conversion of Arylamines to Pinacol Boronates: A Metal-Free Borylation Process
Fanyang Mo et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2010)
Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions
Thomas W. Lyons et al.
CHEMICAL REVIEWS (2010)
Green Chemistry: Principles and Practice
Paul Anastas et al.
CHEMICAL SOCIETY REVIEWS (2010)
Radical Arylation of Phenols, Phenyl Ethers, and Furans
Alexander Wetzel et al.
CHEMISTRY-A EUROPEAN JOURNAL (2010)
tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative
Eiji Shirakawa et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)
Organocatalysis in Cross-Coupling: DMEDA-Catalyzed Direct C-H Arylation of Unactivated Benzene
Wei Liu et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)
An efficient organocatalytic method for constructing biaryls through aromatic C-H activation
Chang-Liang Sun et al.
NATURE CHEMISTRY (2010)
Recent advances in aryl-aryl bond formation by direct arylation
Gerard P. McGlacken et al.
CHEMICAL SOCIETY REVIEWS (2009)
Metal-Free Oxidative Cross-Coupling of Unfunctionalized Aromatic Compounds
Yasuyuki Kita et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2009)
Synthesis of Amino- and Hydroxybiphenyls by Radical Chain Reaction of Arenediazonium Salts
Alexander Wetzel et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)
Oxidative cross-coupling of arenes induced by single-electron transfer leading to biaryls by use of organoiodine(III) oxidants
Toshifumi Dohi et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)
Surprisingly long-lived ascorbyl radicals in acetonitrile: Concerted proton-electron transfer reactions and thermochemistry
Jeffrey J. Warren et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2008)
Potassium t-Butoxide Alone Can Promote the Biaryl Coupling of Electron-Deficient Nitrogen Heterocycles and Haloarenes
Shuichi Yanagisawa et al.
ORGANIC LETTERS (2008)
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
Dino Alberico et al.
CHEMICAL REVIEWS (2007)
Selected patented cross-coupling reaction technologies
Jean-Pierre Corbet et al.
CHEMICAL REVIEWS (2006)
Dantrolene - A review of its pharmacology, therapeutic use and new developments
T Krause et al.
ANAESTHESIA (2004)
Aryl-aryl bond formation one century after the discovery of the Ullmann reaction
J Hassan et al.
CHEMICAL REVIEWS (2002)
Share Paper
