Issue 2, 2005
From the journal:

Organic & Biomolecular Chemistry

Synthesis and stereochemistry of musacins isolated from Streptomyces griseoviridis (FH-S 1832)

Toshihiko Uekia  and  Takamasa Kinoshita*a  

* Corresponding authors

a Department of Chemistry, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka, Japan

Abstract

Musacins E (1a), B1 (2a) and B2 (3a) have been synthesized starting from D-erythronolactone, L-tartaric acid and (S)-malic acid. The absolute stereochemistry of musacins was unambiguously established by this synthesis.

Graphical abstract: Synthesis and stereochemistry of musacins isolated from Streptomyces griseoviridis (FH-S 1832)

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Article information

DOI
https://doi.org/10.1039/B415759C
Article type
Paper
Submitted
11 Oct 2004
Accepted
24 Nov 2004
First published
14 Dec 2004

Org. Biomol. Chem., 2005,3, 295-302

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Synthesis and stereochemistry of musacins isolated from Streptomyces griseoviridis (FH-S 1832)

T. Ueki and T. Kinoshita, Org. Biomol. Chem., 2005, 3, 295 DOI: 10.1039/B415759C

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