Issue 17, 1982

Energy barriers to the enantiotopomerisation of tetrahedral boron chelates: a rearrangement of some cyclic boron compounds

Abstract

The racemisation of dissymmetric diarylboron salicylideneaminato-chelates involves B–N bond dissociation and a planar trico-ordinate boron atom, rather than planar tetraco-ordinate boron as was recently suggested.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 1008-1009

Energy barriers to the enantiotopomerisation of tetrahedral boron chelates: a rearrangement of some cyclic boron compounds

A. J. Boulton and C. S. Prado, J. Chem. Soc., Chem. Commun., 1982, 1008 DOI: 10.1039/C39820001008

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