Issue 45, 2008

Unprecedented biological cyclopropanation in the biosynthesis of FR-900848

Abstract

We were able to show the predominant incorporation of a single enantiomer and intact incorporation of multiply labelled synthetic diketide precursors (14 and 16), which established the intermediacy of cyclopropanated diketide and led to our proposal for the unprecedented biological cyclopropanation, viaPKS (polyketide synthase) having a novel cyclopropanase domain, in the biosynthesis of FR-900848 (1).

Graphical abstract: Unprecedented biological cyclopropanation in the biosynthesis of FR-900848

Supplementary files

Article information

Article type
Communication
Submitted
06 Jun 2008
Accepted
12 Sep 2008
First published
14 Oct 2008

Chem. Commun., 2008, 6016-6018

Unprecedented biological cyclopropanation in the biosynthesis of FR-900848

T. Tokiwano, H. Watanabe, T. Seo and H. Oikawa, Chem. Commun., 2008, 6016 DOI: 10.1039/B809610D

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