Issue 7, 1986

Tungsten Wittig reagents: an efficient synthesis of α-functionalised tri- and tetrasubstituted alkenes

Abstract

The reaction of tungsten alkylidene complexes of the type W([double bond, length half m-dash]CR1R2)X2Y2 with organic carbonyl groups is shown to enable a variety of di-, tri-, and tetra-substituted alkenes to be synthesised directly, including enol ethers and enamines.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 531-533

Tungsten Wittig reagents: an efficient synthesis of α-functionalised tri- and tetrasubstituted alkenes

A. Aguero, J. Kress and J. A. Osborn, J. Chem. Soc., Chem. Commun., 1986, 531 DOI: 10.1039/C39860000531

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