Results 291 to 300 of about 408,472 (346)
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Recent advances in aryl–aryl bond formation by direct arylation

Chemical Society Reviews, 2009
The abundance of the biaryl structural motif in natural products, in biologically active molecules and in materials chemistry has positioned aryl-aryl (Ar-Ar) bond formation high on the agenda of synthetic chemists. For decades well-known reactions such as the Mizoroki-Heck and Suzuki-Miyaura have been the methods of choice to furnish biaryls.
Gerard P Mcglacken, Lorraine M Bateman
exaly   +3 more sources

Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation

Chemical Reviews, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Mark Lautens
exaly   +3 more sources

Palladium-Catalyzed Aryl–Aryl Coupling

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
ANASTASIA L, NEGISHI E
openaire   +3 more sources

Aryl Diazonium Salts: Powerful Arylating Agents for Catellani-Type ortho-Arylation

The Journal of Organic Chemistry, 2021
The Catellani reaction provides an efficient synthetic approach to polyfunctionalized arenes. However, the selective ortho-arylating reagents employed in these reactions have been strictly limited to activated bromoarenes. As demonstrated in this work, aryl diazonium salts bearing both electron-donating and electron-withdrawing substituents, after in ...
Ying Fu, Yu-Xia Zhang, Liang-Liang Guo
openaire   +2 more sources

N‐Arylation of Diketopyrrolopyrroles with Aryl Triflates

Chemistry – An Asian Journal, 2020
AbstractA new methodology for the double N‐arylation of diketopyrrolopyrroles with aryl triflates has been developed. It is now possible to prepare diketopyrrolopyrroles bearing N‐substituents derived from naphthalene, anthracene and coumarin in two steps from commercially available phenols. This represents the first time arenes lacking strong electron‐
Krzysztof Gutkowski   +4 more
openaire   +3 more sources

Dilithium Aryl Cyanocuprates from Butyl Aryl Tellurides.

ChemInform, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Priscila Castelani   +2 more
openaire   +1 more source

Arylation of Aldehyde Homoenolates with Aryl Bromides

Organic Letters, 2013
A mild palladium catalyzed coupling of reactive aldehyde homoenolates with aryl bromides is described. Aldehyde homoenolates are generated by ring opening of cyclopropanols via a C-C cleavage step. The coupling generates aldehyde products at room temperature in 59-93% yield.
Kevin, Cheng, Patrick J, Walsh
openaire   +2 more sources

Aryl–aryl coupling via directed lithiation and oxidation

Chemical Communications, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
David S, Surry   +3 more
openaire   +2 more sources

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