Issue 0, 1979

Reactions of phosphines with acetylenes. Part 18. The mechanism of formation of 1,2-alkylidenediphosphoranes

Abstract

The reactions of dimethyl acetylenedicarboxylate and dibenzoylacetylene with a variety of tertiary arylphosphines, in excess, have been studied. Evidence is presented to show that 1,2-alkylidenediphosphoranes are formed via zwitterionic intermediates which have the character of nucleophilic carbenes. 1,2-Bismethoxycarbonyl-2-thioxoethylidenetriphenylphosphorane and 1,2-dibenzoyl-2-thioxoethylidenetriphenylphosphorane have been isolated by trapping the intermediate with sulphur.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 2133-2135

Reactions of phosphines with acetylenes. Part 18. The mechanism of formation of 1,2-alkylidenediphosphoranes

J. C. Tebby, I. F. Wilson and D. V. Griffiths, J. Chem. Soc., Perkin Trans. 1, 1979, 2133 DOI: 10.1039/P19790002133

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