Enzymes in organic synthesis: Lipase catalyzed resolution of secondary α-ketoalcohols
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference18 articles.
1. Stereoselective Synthesis of Diastereomeric Amino Alcohols from Chiral Aminocarbonyl Compounds by Reduction or by Addition of Organometallic Reagents
2. Effects of neighboring functional groups on 1,2-asymmetric induction in the reduction of ketones with sodium borohydride
3. Stereoselectivity in the reduction of aliphatic .alpha.-ketols with aluminum hydride reagents
4. Aluminum hydride reduction of .alpha.-ketols. II. Additional evidence for conformational flexibility in the transition state
5. An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction
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3. ChemInform Abstract: Enzymes in Organic Synthesis: Lipase-Catalyzed Resolution of Secondary α-Ketoalcohols.;ChemInform;2010-08-20
4. Asymmetric Synthesis of Aliphatic 2-Hydroxy Ketones by Enzymatic Carboligation of Aldehydes;European Journal of Organic Chemistry;2007-06
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