Issue 16, 1992

A new synthesis of α-fluoro-α,β-unsaturated ketones and esters based on organoselenium methodology

Abstract

Fluoroselenenylation of α-diazoketones and α-diazoesters using a phenylselenenyl fluoride equivalent, generated in situ from phenylselenenyl bromide and AgF, followed by oxidation with hydrogen peroxide, provided α-fluoro-α,β-unsaturated ketones and ester, respectively, in moderate yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 1148-1150

A new synthesis of α-fluoro-α,β-unsaturated ketones and esters based on organoselenium methodology

Y. Usuki, M. Iwaoka and S. Tomoda, J. Chem. Soc., Chem. Commun., 1992, 1148 DOI: 10.1039/C39920001148

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