Journal ArticleOPEN ACCESS

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

Bioscience, Biotechnology and Biochemistry (2014) 78(5) 766-769
DOI: 10.1080/09168451.2014.905192
6Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Author supplied keywords

Cite

CITATION STYLE

APA

Saito, A., Igarashi, W., Furukawa, H., Yamada, T., Kuwahara, S., & Kiyota, H. (2014). Facile synthesis of the cyclohexane fragment of enacloxins, a series of antibiotics isolated from Frateuria sp. W-315. Bioscience, Biotechnology and Biochemistry, 78(5), 766–769. https://doi.org/10.1080/09168451.2014.905192

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free