Determination of the Absolute Configurations of the Anteiso Acid Moieties of Glycoglycerolipid S365A Isolated from Corynebacterium aquaticum-Reference-Cited by-同舟云学术

Determination of the Absolute Configurations of the Anteiso Acid Moieties of Glycoglycerolipid S365A Isolated from Corynebacterium aquaticum

Published:2002-01-01 Issue:8 Volume:66 Page:1719-1722
ISSN:0916-8451
Container-title:Bioscience, Biotechnology, and Biochemistry
language:en
Short-container-title:Bioscience, Biotechnology, and Biochemistry

Author:

AKASAKA Kazuaki¹,SHICHIJYUKARI Seiya¹,MEGURO Hiroshi²,OHRUI Hiroshi¹

Affiliation:

1. Graduate School of Life Sciences, Tohoku University Tsutsumidori-Amamiyamachi 1-1, Aobaku, Sendai 981-8555, Japan

2. Tohoku Fukushi University Kunimi, Aobaku, Sendai 981-0943, Japan

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

Link

https://www.tandfonline.com/doi/pdf/10.1271/bbb.66.1719

Reference13 articles.

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2. 2) Ariens, E. J., Stereochemistry, a basis for sophisticated nonsense in pharmacokinetics and clinical pharmacology. Euro. J. Clin. Pharmacol. 26, 663-668 (1984).

3. 3) Drayer, D. E., Pharmacodynamic and pharmacokinetic differences between druige enantiomers in humans: an overview. Clin. Pharmacol. Ther. 40, 125-133 (1986).

4. 4) Costantino, V., Fattorisso, E., and Mangoni, A., Isolation of five-membered cyclitol glycolipids, crasserides: unique glycerides from the sponge Pseudoceratina crassa. J. Org. Chem. 58, 186-191 (1993).

5. 5) Mori, K., Harada, H., Zagatti, P., Cork, A., and Hall, D. R., Pheromone synthesis. CXXVI. Synthesis and biological activity of four stereoisomers of 6,10,14-trimethyl-2-pentadecanol, the female-produced sex pheromone of rice moth (Corcyra cephalonica) and its stereoisomers. Liebigs Ann. Chem., 259-267 (1991).

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