Literature DB >> 2766432

A gas-liquid chromatographic method for steric analysis of epoxy acids.

P Fahlstadius1, M Hamberg.   

Abstract

A gas-liquid chromatographic method for determination of the absolute configuration of the two chiral carbon atoms of epoxy fatty acids was developed. The method involved (1) conversion of the saturated epoxy ester into a pair of regioisomeric allylic alcohols by consecutive treatments with selenophenoxide anion and hydrogen peroxide, (2) oxidative ozonolysis performed on the (-)-menthoxycarbonyl derivatives of the allylic alcohols, and (3) steric analysis of the resulting two 2-hydroxy acids (methyl esters, (-)-menthoxycarbonyl derivatives) by gas-liquid chromatography using appropriate reference compounds. Application of the method for steric analysis of several synthetic epoxyoctadecanoates as well as (+)-vernolic acid derived from Vernonia galamensis is described.

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Year:  1989        PMID: 2766432     DOI: 10.1016/0009-3084(89)90061-3

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


  3 in total

Review 1.  Bisallylic hydroxylation and epoxidation of polyunsaturated fatty acids by cytochrome P450.

Authors:  E H Oliw; J Bylund; C Herman
Journal:  Lipids       Date:  1996-10       Impact factor: 1.880

2.  On the Specificity of a Fatty Acid Epoxygenase in Broad Bean (Vicia faba L.).

Authors:  M Hamberg; P Fahlstadius
Journal:  Plant Physiol       Date:  1992-07       Impact factor: 8.340

3.  Peroxygenase-Catalyzed Fatty Acid Epoxidation in Cereal Seeds (Sequential Oxidation of Linoleic Acid into 9(S),12(S),13(S)-Trihydroxy-10(E)-Octadecenoic Acid).

Authors:  M. Hamberg; G. Hamberg
Journal:  Plant Physiol       Date:  1996-03       Impact factor: 8.340

  3 in total

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