Literature DB >> 17388595

Rationale behind the resistance of dialkylbiaryl phosphines toward oxidation by molecular oxygen.

Timothy E Barder1, Stephen L Buchwald.   

Abstract

Electron-rich dialkylbiaryl phosphines, which comprise a common class of supporting ligands for Pd-catalyzed cross-coupling reactions, are highly resistant toward oxidation by molecular oxygen. Presented herein are possible reasons why this class of phosphine ligands manifests this property. Experimental and theoretical data suggest that the two alkyl substituents on the phosphorus center and the 2' and 6' positions of the biaryl backbone play an important role in inhibiting oxidation of this class of ligands.

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Year:  2007        PMID: 17388595     DOI: 10.1021/ja0683180

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  13 in total

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5.  Chiral allene-containing phosphines in asymmetric catalysis.

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8.  Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.

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Journal:  Acc Chem Res       Date:  2008-11-18       Impact factor: 22.384

9.  Chemically triggered crosslinking with bioorthogonal cyclopropenones.

Authors:  R David Row; Sean S Nguyen; Andrew J Ferreira; Jennifer A Prescher
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10.  Biaryl Monophosphine Ligands in Palladium-Catalyzed C-N Coupling: An Updated User's Guide.

Authors:  Bryan T Ingoglia; Corin C Wagen; Stephen L Buchwald
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