Enzymatic Synthesis of Enantiomerically Pure Chiral Synthons: Lipase-Catalyzed Resolution of (R/S, 4E)-2-Methyl-4-hexen-l-ol
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1991-34721.pdf
Cited by 11 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. ChemInform Abstract: Enzymatic Synthesis of Enantiomerically Pure Chiral Synthons: Lipase- Catalyzed Resolution of (R/S,4D)-2-Methyl-4-hexen-1-ol.;ChemInform;2010-08-22
2. Approaches based on enzyme mediated kinetic to dynamic kinetic resolutions: A versatile route for chiral intermediates;Coordination Chemistry Reviews;2008-03
3. Zirconium-Catalyzed Asymmetric Carboalumination of Alkenes: ZACA–Lipase-Catalyzed Acetylation Synergy;Advanced Synthesis & Catalysis;2007-03-05
4. Biocatalysis as a new powerful tool for the synthesis of enantiomerically pure chiral building blocks;Advances in Asymmetric Synthesis Volume 2;1997
5. Enzymatic resolutions of alcohols, esters, and nitrogen-containing compounds;Enzymatic Reactions in Organic Media;1996
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