Asymmetric reactions. XI. Sterical course of enzymatic reduction of methyl alkyl ketones and methyl aryl ketones-Reference-Cited by-同舟云学术

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Asymmetric reactions. XI. Sterical course of enzymatic reduction of methyl alkyl ketones and methyl aryl ketones

Published:1966 Issue:6 Volume:31 Page:2615-2618
ISSN:0010-0765
Container-title:Collection of Czechoslovak Chemical Communications
language:en
Short-container-title:Collect. Czech. Chem. Commun.

Author:

Červinka O.,Hub L.

Publisher

Institute of Organic Chemistry & Biochemistry

Subject

General Chemistry

Cited by 22 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

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3. Preliminary investigation of the yeast-mediated reduction of β-keto amides derived from cyclic amines as potential resolution methodology;Tetrahedron: Asymmetry;2008-04

4. Enantioselective production of halohydrin precursor of Propranolol catalysed by immobilized yeasts;Journal of Molecular Catalysis B: Enzymatic;2005-11

5. Highly stereoselective reduction of haloketones using three new yeasts: application to the synthesis of (S)-adrenergic β-blockers related to propranolol;Tetrahedron: Asymmetry;2004-03

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