Issue 14, 1975

The mechanism of the Stevens rearrangement

Abstract

The influence of solvent viscosity and reaction temperature upon the stereoselectivity and intramolecularity of the Stevens [1,2] rearrangement of the ylide (1) has been examined; the results are compatible with two possible mechanisms: (i) a radical pair mechanism with an average geminate recombination rate which is exceptionally fast, or (ii) dual pathways involving concurrent radical pair and concerted processes.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 543-545

The mechanism of the Stevens rearrangement

W. D. Ollis, M. Rey, I. O. Sutherland and G. L. Closs, J. Chem. Soc., Chem. Commun., 1975, 543 DOI: 10.1039/C39750000543

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