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Carbon-carbon bond-forming reactions using alkyl fluorides

Authors :
Aki Ikumi
Hiroyasu Watabe
Yoshiaki Shinohara
Hirohisa Todo
Nobuaki Kambe
Jun Terao
Source :
Pure and Applied Chemistry. 80:941-951
Publication Year :
2008
Publisher :
Walter de Gruyter GmbH, 2008.

Abstract

This account reviews C-C bond formation reactions using alkyl fluorides mostly focusing on the transition-metal-catalyzed reactions. These reactions proceed efficiently under mild conditions by the combined use of Grignard reagents and transition-metal catalysts, such as Ni, Cu, and Zr. It is proposed that ate complex intermediates formed by the reaction of these transition metals with Grignard reagents play important roles as the active catalytic species. Organoaluminun reagents react directly with alkyl fluorides in nonpolar solvents at room temperature to form C-C bonds. These studies demonstrate the practical usefulness of alkyl fluorides in C-C bond formation reactions and provide a promising method for the construction of carbon frameworks employing alkyl fluorides. The scope and limitations, as well as reaction pathways, are discussed.

Details

ISSN :
13653075 and 00334545
Volume :
80
Database :
OpenAIRE
Journal :
Pure and Applied Chemistry
Accession number :
edsair.doi...........7c3ccf05aa8cf255ff6ce7314c7a922a