Issue 5, 1992

Lewis base-induced rearrangement of primary ethyn-1-ylphosphines, a new and efficient route to phosphaalkynes

Abstract

Phosphaalkynes bearing primary carbon substituents are prepared in good yield by low-temperature Lewis base-induced rearrangement of primary ethyn-1-ylphosphines; the mechanism involves a P-unsubstituted phosphaallene intermediate.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 415-416

Lewis base-induced rearrangement of primary ethyn-1-ylphosphines, a new and efficient route to phosphaalkynes

J. Guillemin, T. Janati and J. Denis, J. Chem. Soc., Chem. Commun., 1992, 415 DOI: 10.1039/C39920000415

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