Issue 24, 2000

One pot synthesis of a chiral N-phosphine substituted iminophosphorane: X-ray structure and in situNMR study

Abstract

An X-ray crystal structure reveals that the attempted deprotonation of cyclopropyl(triphenyl)phosphonium bromide with sodium amide affords a chiral N-phosphine substituted iminophosphorane via an unusual mechanism that has been investigated by multi-nuclear and variable temperature in situ NMR spectroscopy.

Supplementary files

Article information

Article type
Communication
Submitted
19 Jul 2000
Accepted
25 Oct 2000
First published
28 Nov 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 4237-4239

One pot synthesis of a chiral N-phosphine substituted iminophosphorane: X-ray structure and in situ NMR study

A. S. Batsanov, M. G. Davidson, I. Fernández, J. A. K. Howard, F. López-Ortiz and R. D. Price, J. Chem. Soc., Perkin Trans. 1, 2000, 4237 DOI: 10.1039/B005816P

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