High facial selectivity observed in amine coordination to chiral oxazaborolidinones

Chem Commun (Camb). 2005 Feb 21:(7):859-61. doi: 10.1039/b413370f. Epub 2004 Dec 16.

Abstract

A variety of 1,3,2-oxazaborolidin-5-ones (OXB) derived from N-sulfonyl amino acids exhibit a high top-face selectivity in complexation with pyridines under thermodynamically controlled conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry*
  • Boron Compounds / chemical synthesis*
  • Boron Compounds / chemistry*
  • Magnetic Resonance Spectroscopy / methods
  • Models, Molecular
  • Molecular Conformation
  • Sensitivity and Specificity
  • Stereoisomerism

Substances

  • Amines
  • Boron Compounds