Issue 22, 1983

Peterson olefination using phenylsulphonyltrimethylsilylmethane. A new preparation of vinylic sulphones

Abstract

The anion from phenylsulphonyltrimethylsilylmethane reacts, in 1,2-dimethoxyethane at –78 °C, with both aldehydes and ketones to give the corresponding alkenyl phenyl sulphones in good yield.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1281-1282

Peterson olefination using phenylsulphonyltrimethylsilylmethane. A new preparation of vinylic sulphones

S. V. Ley and N. S. Simpkins, J. Chem. Soc., Chem. Commun., 1983, 1281 DOI: 10.1039/C39830001281

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