Skip to main content
Article thumbnail
Location of Repository

Enantioselectivity in microbial reduction of prochiral carbonyl groups: a wide screening toward R and S isomers

By G. FANTIN, M. FOGAGNOLO, A. MEDICI, P. PEDRINI, S. POLI, F. GARDINI and M. E. GUERZONI

Abstract

More than fifty yeast and mould strains were tested in the reduction of 2-acylthiazoles. the possibility of obtaining R and S enantiomers with high enantioselectivities from various species and starins is described

Topics: 2-Acylthiazole, microbial reduction, homochiral alchohols
Publisher: PERGAMON-ELSEVIER SCIENCE LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD, ENGLAND, OX5 1GB
Year: 1991
OAI identifier: oai:iris.unife.it:11392/462453
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • http://hdl.handle.net/11392/46... (external link)
  • Suggested articles


    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.