Reactions of a N-Acyliminium Ion Pool with Benzylsilanes. Implication of a Radical/Cation/Radical Cation Chain Mechanism Involving Oxidative C−Si Bond Cleavage
Journal of the American Chemical Society2007Vol. 129(7), pp. 1902–1903
Citations Over TimeTop 10% of 2007 papers
Abstract
The reaction of a N-acyliminium ion pool with benzylsilane proceeds by a chain mechanism involving oxidative C−Si bond cleavage. A radical/cation/radical cation crossover mechanism involving single electron transfer has been proposed. The effective binary system consisting of a stoichiometric amount of a benzylsilane and a catalytic amount of a more easily oxidized benzylstannane has been developed.
Related Papers
- → Photo-oxidation of polymers—Part V: A new chain scission mechanism in polyolefins(1982)95 cited
- → A computational study on thermal decomposition mechanism of β-1 linkage lignin dimer(2014)42 cited
- → Pyrylogens: Synthesis, Structural, Electrochemical, and Photophysical Characterization of a New Class of Electron Transfer Sensitizers(2008)32 cited
- → Theoretical considerations of scission and endlinking reactions in irradiated polymers(1987)2 cited
- → Chain Scission Efficiency in the Oxidation of Natural Rubber Vulcanizates(1957)