Enantioselective preparation of α-acyloxy ketones from α-hydroxy and α-amino acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. A very mild, catalytic and versatile procedure for α-oxidation of ketone silyl enol ethers using (salen)manganese(III) complexes; a new, chiral complex giving asymmetric induction. A possible model for selective biochemical oxidative reactions through enol formation
2. ASYMMETRIC REDUCTION OF BENZIL TO BENZOIN CATALYZED BY THE ENZYME SYSTEM OF A MICROORGANISM
3. L-Lactate dehydrogenase: substrate specificity and use as a catalyst in the synthesis of homochiral 2-hydroxy acids
4. Chemistry of oxaziridines. 14. Asymmetric oxidation of ketone enolates using enantiomerically pure (camphorylsulfonyl)oxaziridine
5. Remarkable optical induction in the reduction of .alpha.-oxo esters with B-(3-pinanyl)-9-borabicyclo[3.3.1]nonane. Synthesis of .alpha.-hydroxy esters of 100% optical purity
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