Stereospecific microbial reduction of ethyl 1-benzyl-3-oxo-piperidine-4-carboxylate-Reference-Cited by-同舟云学术

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Stereospecific microbial reduction of ethyl 1-benzyl-3-oxo-piperidine-4-carboxylate

Published:2006-08 Issue:13 Volume:17 Page:2015-2020
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Guo Zhiwei,Patel Bharat P.,Corbett Richard M.,Goswami Animesh,Patel Ramesh N.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference7 articles.

1. Purification and Cloning of a Ketoreductase used for the Preparation of Chiral Alcohols

2. Asymmetric reduction of a variety of ketones with a recombinant carbonyl reductase: identification of the gene encoding a versatile biocatalyst

3. Enantioselective reduction of carbonyl compounds by whole-cell biotransformation, combining a formate dehydrogenase and a (R)-specific alcohol dehydrogenase

4. Dehydrogenases and transaminases in asymmetric synthesis

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enzymatic reduction of α-substituted ketones with concomitant dynamic kinetic resolution;Journal of Molecular Catalysis B: Enzymatic;2016-11

2. Dynamic Kinetic Resolutions Based on Reduction Processes;Synthetic Methods for Biologically Active Molecules;2013-08-30

3. A compendium of cyclic sugar amino acids and their carbocyclic and heterocyclic nitrogen analogues;Amino Acids;2013-08-18

4. Synthetic approaches to a chiral 4-amino-3-hydroxy piperidine with pharmaceutical relevance;Organic & Biomolecular Chemistry;2012

5. Enzyme Catalysis in the Synthesis of Active Pharmaceutical Ingredients;Enzyme Technologies;2011-05-25

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