Rate and Mechanism of the Oxidative Addition of Vinyl Triflates and Halides to Palladium(0) Complexes in DMF
Author:
Affiliation:
1. Ecole Normale Supérieure, Département de Chimie, UMR CNRS 8640, 24 Rue Lhomond, F-75231 Paris Cedex 5. France
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om030298c
Reference30 articles.
1. Rate and Mechanism of Oxidative Addition of Aryl Triflates to Zerovalent Palladium Complexes. Evidence for the Formation of Cationic (.sigma.-Aryl)palladium Complexes
2. Nickel- and Palladium-Catalyzed Homocoupling of Aryl Triflates. Scope, Limitation, and Mechanistic Aspects
3. Factors Affecting the Oxidative Addition of Aryl Electrophiles to 1,1‘-Bis(diphenylphosphino)ferrocenepalladium(η2-methyl acrylate), an Isolable Pd[0] Alkene Complex
4. Mechanistic Studies on Oxidative Addition of Aryl Halides and Triflates to Pd(BINAP)2 and Structural Characterization of the Product from Aryl Triflate Addition in the Presence of Amine
5. Palladium-catalysed vinylation of enol triflates
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