Issue 14, 1993

The conformation of derivatives of O-aryllactic acid used as chiral reagents in structure determination. NMR and X-ray structure analysis of diastereoisomeric menthol esters

Abstract

The 1H NMR analysis of O-aryllactic esters allows the attribution of the absolute configuration to alcohols according to a new model with Hα in the acid plane in a hitherto unprecedented conformation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1113-1115

The conformation of derivatives of O-aryllactic acid used as chiral reagents in structure determination. NMR and X-ray structure analysis of diastereoisomeric menthol esters

A. Heumann, J. Chem. Soc., Chem. Commun., 1993, 1113 DOI: 10.1039/C39930001113

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