Preparation and stereochemical integrity of certain thioesters of 2-arylpropionic acids and related compounds

Author:

Hanrahan Patrick E1,Moynihan Humphrey A1

Affiliation:

1. Department of Chemistry/Analytical and Biological Chemistry Research Facility, University College Cork, Cork, Ireland

Abstract

Abstract 2-Arylpropionate thioesters 5, 6a/6b and 7a/7b, 2-aryloxypropionate thioesters 8a/8b and 2-alkoxy-2-arylacetate thioesters 9a/9b were prepared from thiol 4 and the corresponding carboxylic acids. Thioesters 6a/6b, 7a/7b, 8a/8b and 9a/9b were monitored for evidence of inter-conversion between epimers in acetonitrile solvent at 40°C, by optical activity in the cases of 6a/6b and 7a/7b, and by 1H NMR spectroscopy in the cases of 8a/8b and 9a/9b. Only in the case of thioesters 9a/9b was significant inter-conversion between epimers observed.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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