Synthesis of enantiomerically pure (R)-and (S)-1-benzoyloxypropane-2,3-diol and revision of the stereochemical outcome of the Candida antarctica lipase-catalyzed benzoylation of glycerol-Reference-Cited by-同舟云学术

Synthesis of enantiomerically pure (R)-and (S)-1-benzoyloxypropane-2,3-diol and revision of the stereochemical outcome of the Candida antarctica lipase-catalyzed benzoylation of glycerol

Published:2011-03 Issue:6 Volume:22 Page:658-661
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Casati Silvana,Ciuffreda Pierangela,Santaniello Enzo

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. Chiral 1,2-diphosphine ligands. Synthesis and application to rhodium-catalyzed asymmetric hydrogenations

2. New precursors for preparing organic conducting materials: synthesis of (R)-hydroxymethylbis(ethylenedithio)tetrathiafulvalene, and the ring expansion of a cyclic sulfate ester

3. An Optimized Protein Kinase C Activating Diacylglycerol Combining High Binding Affinity (Ki) with Reduced Lipophilicity (log P)

4. Enantioselective Microbial Reduction of Monoesters of 1,3-Dihydroxypropanone: Synthesis of (S)- and (R)-1,2-O-Isopropylideneglycerol

5. Baker's yeast mediated reduction of dihydroxyacetone derivatives

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