Chiral synthesis of a triglyceride: example of 1-butyroyl 2-oleoyl 3-palmitoyl sn glycerol
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry
Reference14 articles.
1. Synthesis of 100-gram quantities of highly purified mixed acid triglycerides
2. Synthesis of enantiomerically pure glyceryl esters and ethers. II. Methods employing the precursor 3,4-isopropylidene-D-mannitol
3. The synthesis of Chiral Glycerides starting from D- and L-serine
4. A short highly regio- and stereoselective synthesis of triacylglycerols
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2. Regioselective and Stereospecific Halosilylating Cleavage of the Oxirane System of Glycidol Derivatives as an Efficient Strategy to C2-O-Functionalized C3-Vicinal Halohydrins;European Journal of Organic Chemistry;2008-05
3. Regioselective and stereospecific acylation across oxirane- and silyloxy systems as a novel strategy to the synthesis of enantiomerically pure mono-, di- and triglycerides;Organic & Biomolecular Chemistry;2007
4. Regioselective and stereospecific cleavage of a terminal oxirane system: A novel synthetic approach to lipid mediator congeners—1,2(2,3)-diacyl-3(1)-halo-sn-glycerols;Bioorganic & Medicinal Chemistry Letters;2006-07
5. Investigation of crude latex from variousCarica papayavarietices for lipid bioconversions;Journal of the American Oil Chemists' Society;2000-08
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