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-Reference-Cited by-同舟云学术

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

Published:2022-01-31 Issue:5-6 Volume:48 Page:554-568
ISSN:0098-0331
Container-title:Journal of Chemical Ecology
language:en
Short-container-title:J Chem Ecol

Author:

Akasaka Kazuaki^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry,Ecology, Evolution, Behavior and Systematics,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s10886-021-01345-z.pdf

Reference73 articles.

1. Akasaka K, Meguro H, Ohrui H (1997) Enantiomeric separation of carboxylic acids having chiral centers remote from the carboxyl group by labelling with a chiral fluorescent derivatization reagent. Tetrahedron Lett. 38:6853–6856. https://doi.org/10.1016/S0040-4039(97)01616-X

2. Akasaka K, Imaizumi K, Ohrui H (1998) Enantiomeric separation of branched fatty acids having chiral centers remote from the carboxyl group by labelling with chiral fluorescent derivatization reagents. Enantiomer 3:169–174

3. Akasaka K, Ohrui H (1999) Enantiomeric separation of branched fatty acids after conversion with trans-2-(2,3-anthracenedicarboximido)cyclohexanol, a highly sensitive chiral fluorescent conversion reagent. Biosci Biotechnol Biochem 63:1209–1215. https://doi.org/10.1271/bbb.63.1209

4. Akasaka K, Shichijyukari S, Matsuoka S, Murata M, Meguro H, Ohrui H (2000) Absolute configuration of a ceramide with a novel branched-chain fatty acid isolated from the epiphytic dinoflagellate, Coolia monotis. Biosci Biotechnol Biochem 64:1842–1846. https://doi.org/10.1271/bbb.64.1842

5. Akasaka K, Shichijyukari S, Ohrui H, Meguro H (2002) Determination of the absolute configurations of the anteiso acid moieties of glycoglycerolipid S365A isolated from Corynebacterium aquaticum. Biosci Biotechnol Biochem 66:1719–1722. https://doi.org/10.1271/bbb.66.1719

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1. Tribute to Professor Kenji Mori and his contribution to Chemical Ecology;Journal of Chemical Ecology;2022-06