Literature DB >> 12353633

Determination of the absolute configurations of the anteiso acid moieties of glycoglycerolipid S365A isolated from Corynebacterium aquaticum.

Kazuaki Akasaka1, Seiya Shichijyukari, Hiroshi Meguro, Hiroshi Ohrui.   

Abstract

The absolute configurations of the two acid moieties, 12-methyltetradecanoate and 14-methylhexadecanoate, of glycoglycerolipid S365A isolated from Corynebacterium aquaticum were determined by an HPLC analysis after their conversion with the chiral fluorescent labeling reagents, (1S,2S)- and (1R,2R)-2-(2,3-anthracenedicarboximido)cyclohexanol. Both anteiso acids had the S configuration.

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Year:  2002        PMID: 12353633     DOI: 10.1271/bbb.66.1719

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  3 in total

1.  Enantioselective analysis of chiral anteiso fatty acids in the polar and neutral lipids of food.

Authors:  Simone Hauff; Georg Hottinger; Walter Vetter
Journal:  Lipids       Date:  2010-03-12       Impact factor: 1.880

Review 2.  A Highly Selective and Sensitive Chiral Derivatization Method for High- Performance Liquid Chromatographic Determination of the Stereoisomer Composition of Natural Products With Chiral Branched Alkyl Chains.

Authors:  Kazuaki Akasaka
Journal:  J Chem Ecol       Date:  2022-01-31       Impact factor: 2.793

3.  Direct determination of the stereoisomeric composition of callosobruchusic acid, the copulation release pheromone of the azuki bean weevil, Callosobruchus chinensis L., by the 2D-Ohrui-Akasaka method.

Authors:  Arata Yajima; Kazuaki Akasaka; Masamichi Yamamoto; Sachiko Ohmori; Tomoo Nukada; Goro Yabuta
Journal:  J Chem Ecol       Date:  2007-07       Impact factor: 2.793

  3 in total

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