Literature DB >> 1814641

Regio- and stereoselective enzymatic esterification of glycerol and its derivatives.

A W Mazur1, G D Hiler, S S Lee, M P Armstrong, J D Wendel.   

Abstract

A methodology for regio- and stereoselective preparation of acyl glycerol derivatives is presented. It offers easy access to specific 1,2-, 1,3-diglycerides and triglycerides as well as alkyl glycerol esters, phospholipids and glycolipids. These compounds are prepared by esterification of the corresponding glycerol derivatives such as 2-monoglycerides, alkyl glycerols, glyceryl glycosides, glyceryl phosphate esters, or unsubstituted glycerol. The regio- and stereoselectivity in the esterification is achieved by using fatty acid anhydrides and an enzymatic catalyst, 1,3-specific lipase. NMR methods for determining the regio- and stereoselectivity of esterification are discussed.

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Year:  1991        PMID: 1814641     DOI: 10.1016/0009-3084(91)90041-9

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  4 in total

1.  Determination of positional distribution of butyryl groups in milkfat triacylglycerols, triacylglycerol mixtures, and isolated positional isomers of triacylglycerols by gas chromatography and 1H nuclear magnetic resonance spectroscopy.

Authors:  P Kalo; A Kemppinen; I Kilpeläinen
Journal:  Lipids       Date:  1996-03       Impact factor: 1.880

2.  Studies of lipase-catalyzed esterification reactions of some acetylenic fatty acids.

Authors:  M S Lie Ken Jie; F Xun
Journal:  Lipids       Date:  1998-01       Impact factor: 1.880

3.  Enzymatic hydrolysis of long-chain N-heterocyclic fatty esters.

Authors:  M S Lie Ken Jie; M S Syed-Rahmatullah
Journal:  Lipids       Date:  1995-11       Impact factor: 1.880

Review 4.  Synthesis of lysophospholipids.

Authors:  Paola D'Arrigo; Stefano Servi
Journal:  Molecules       Date:  2010-03-08       Impact factor: 4.411

  4 in total

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