Regiospecificity and Enantiospecificity in Microbiological Reduction of Acyclic β-Diketones
Author:
Affiliation:
1. Laboratoire de Chimie Organique Biologique, URA 485 du CNRS, Université Blaise Pascal, 63177, Aubière, Cedex, France
Publisher
Informa UK Limited
Subject
General Agricultural and Biological Sciences,Biochemistry,Biotechnology,Catalysis
Link
https://www.tandfonline.com/doi/pdf/10.3109/10242429008992052
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3. The activities of hydrogenase and enoate reductase in two Clostridium species, their interrelationship and dependence on growth conditions
4. Use of biological systems for the preparation of chiral molecules. 3. Application in pheromone synthesis: preparation of sulcatol enantiomers
5. Utilisation des methodes biologiques pour la preparation de synthons chiraux : I-reduction de β-dicetones acycliques par saccharomyces cerevisiae (levure de boulanger)
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