Microbial and enzymatic approaches to chiral β- and γ-nitro alcohols
- 31 July 1992
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 3 (7) , 947-952
- https://doi.org/10.1016/s0957-4166(00)82192-8
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Enantioselectivity in microbial reduction of prochiral carbonyl groups: A wide screening toward R and S isomersTetrahedron: Asymmetry, 1991
- Asymmetric synthesis of a pheromone for Andrena haemorrhoa F from a chiral nitro alcohol obtained by the yeast reduction of a nitro ketoneTetrahedron, 1990
- (S)-5-Nitro-2-pentanol durch Reduktion mit BäckerhefeEuropean Journal of Organic Chemistry, 1989
- Asymmetric reduction of β- and γ-nitro ketones by bakers' yeastTetrahedron Letters, 1988
- Role of lipase activators produced by Saccharomycopsis lipolytica and calcium ion in its lipase reaction.Agricultural and Biological Chemistry, 1986