Facile synthesis of the cyclohexane fragment of enacloxins, a series of antibiotics isolated from Frateuria sp. W-315-Reference-Cited by-同舟云学术

Facile synthesis of the cyclohexane fragment of enacloxins, a series of antibiotics isolated from Frateuria sp. W-315

Published:2014-05-04 Issue:5 Volume:78 Page:766-769
ISSN:0916-8451
Container-title:Bioscience, Biotechnology, and Biochemistry
language:en
Short-container-title:

Author:

Saito Aki¹,Igarashi Wataru¹,Furukawa Hiroyuki¹,Yamada Teiko¹,Kuwahara Shigefumi¹,Kiyota Hiromasa²

Affiliation:

1. Graduate School of Agricultural Science, Tohoku University, Aoba-ku, Japan

2. Graduate School of Environmental & Life Science, Okayama University, Kita-ku, Japan

Abstract

Abstract An efficient and good yield synthesis of the cyclohexane moiety of enacyloxins, a series of antibiotics isolated from Frateuria sp. W-315, was achieved from d-quinic acid using a successive Barton–McCombie deoxygenation.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/bbb/article-pdf/78/5/766/36799657/bbb0766.pdf

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3. Enacyloxin IIa pinpoints a binding pocket of elongation factor Tu for development of novel antibiotics;Parmeggiani;J. Biol. Chem,2006

4. Antibiotic inhibitors of organellar protein synthesis in Plasmodium falciparum;Clough;Tetrahedron,2002

5. Absolute configuration of the cyclohexane ring part of enacyloxins, a series of antibiotics from Frateuria sp. W-315;Fujimori;Heterocycl. Commun,2001

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