Determination of enantiomeric excess of ethyl 3,5-dihydroxy-6-benzyloxy hexanoate by chiral reverse phase high performance liquid chromatography
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Reference10 articles.
1. Practical Large Scale Synthesis of tert-Butyl (3R,5S)-6-Hydroxy-3,5-O-isopropylidene-3,5-dihydroxyhexanoate: Essential Building Block for HMG-CoA Reductase Inhibitors
2. A facile entry to β,δ-diketo and syn-β,δ-dihydroxy esters
3. Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor
4. Chemoenzymatic Synthesis of Building Blocks for Statin Side Chains
5. Advances in biocatalytic synthesis of pharmaceutical intermediates
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1. Recent progress in GeSi electro-absorption modulators;Science and Technology of Advanced Materials;2014-02
2. Preparation of ethyl 3R,5S-6-(benzyloxy)-3,5-dihydroxy-hexanoate by recombinant diketoreductase in a biphasic system;Bioresource Technology;2011-02
3. Comparison of Chiral Chromatography Columns for Pharmaceutical Method Development;Chiral Separation Methods for Pharmaceutical and Biotechnological Products;2010-10-28
4. Control of Optical Limiting of Carbon Nanotube Dispersions by Changing Solvent Parameters;The Journal of Physical Chemistry C;2010-03-10
5. Stereoselective introduction of two chiral centers by a single diketoreductase: an efficient biocatalytic route for the synthesis of statin side chains;Amino Acids;2009-11-16
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