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Synthesis 1987; 1987(1): 28-32
DOI: 10.1055/s-1987-27830
DOI: 10.1055/s-1987-27830
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Enantioselective Reduction of Vicinally Substituted Monocyclic Aldehydes with Horse Liver Alcohol Dehydrogenase; A New Approach to Chiral Alcohols and Aldehydes
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Publikationsverlauf
Publikationsdatum:
20. August 2002 (online)
Optically active, vicinally substituted monocyclic aldehydes and alcohols can be conveniently prepared by enantioselective reduction of racemic aldehydes by means of horse liver alcohol dehydrogenase (HLADH) under kinetically controlled conditions.