Issue 17, 1993

Synthesis and evolution of phosphanylcarbene–borane adducts

Abstract

Photolysis of [bis(dicyclohexylamino)phosphanyl](trimethylsilyl)diazomethane leads to the corresponding stable carbene1b, which reacts with triethylborane affording a borane–carbene adduct2b, characterized by spectroscopy in solution before rearrangement and fragmentation into P-dicyclohexylamino-C-(ethyl)(trimethylsilyl)phosphaalkene3b; trimethylsilyltrifluoromethanesulfonate adds to 1b giving the methylenephosphonium4b.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1354-1355

Synthesis and evolution of phosphanylcarbene–borane adducts

G. Alcaraz, R. Reed, A. Baceiredo and G. Bertrand, J. Chem. Soc., Chem. Commun., 1993, 1354 DOI: 10.1039/C39930001354

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