Issue 3, 1971

Stereospecific free-radical addition of menthyl phenylphosphinate to cyclohexene: evidence for retention of configuration at phosphorus

Abstract

In contradistinction to a recent report that the free-radical addition of menthyl methylphosphinate to alkenes proceeds with inversion of configuration at phosphorus, dibenzoyl peroxide-catalysed addition of menthyl phenylphosphinate to cyclohexene occurs with retention of configuration.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 146-147

Stereospecific free-radical addition of menthyl phenylphosphinate to cyclohexene: evidence for retention of configuration at phosphorus

W. B. Farnham, R. K. Murray and K. Mislow, J. Chem. Soc. D, 1971, 146 DOI: 10.1039/C29710000146

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