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Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2015, Volume 357, Issue 8, pp. 1697 - 1702
Journal Article
Catalysis Communications, ISSN 1566-7367, 07/2017, Volume 97, pp. 5 - 9
The 3-hydroxypiperidine moiety is a privileged scaffold encountered in many bioactive compounds. An NADPH-dependent reductase (YGL039W) from Kluyveromyces... 
Asymmetric reduction | Carbonyl reductase | Cofactor-recycling system | (R)-N-Boc-3-hydroxypiperidine | ACID | ENZYMES | CONSTRUCTION | CHEMISTRY, PHYSICAL | DEHYDROGENASE | Medical colleges | Recycling (Waste, etc.)
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2014, Volume 356, Issue 9, pp. 1943 - 1948
A versatile keto ester reductase CgKR1, exhibiting a broad substrate spectrum, was obtained from Candida glabrata by genome data mining. It showed the highest... 
aromatic α‐keto esters | protein engineering | reductases | substrate specificity | aromatic α-keto esters | ENANTIOSELECTIVITY | STABILITY | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | CARBONYL REDUCTASE | METHYL (R)-O-CHLOROMANDELATE | DIRECTED EVOLUTION | PHOSPHITE DEHYDROGENASE | ENZYMES | aromatic alpha-keto esters | CHEMISTRY, APPLIED | THERMOSTABILITY
Journal Article
Journal Article