Issue 16, 2006
From the journal:

Chemical Communications

Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles†

Takao Ichino,a   Hirokazu Arimoto*b  and  Daisuke Uemura*a  

* Corresponding authors

a Department of Chemistry, Graduate School of Science, and Institute for Advanced Research, Nagoya University, Chikusa, Japan
E-mail: uemura@chem3.chem.nagoya-u.ac.jp
Fax: (+81) 52-789-5041
Tel: (+81) 52-789-3654

b Graduate School of Life Sciences, Tohoku University, Tsutsumidori-Amamiyamachi, Aoba, Japan
E-mail: arimoto@biochem.tohoku.ac.jp
Fax: (+81) 22-717-8806
Tel: (+81) 22-717-8803

Abstract

A novel avenue for oxazoles via Beckmann rearrangement of α-formyl ketoxime dimethyl acetals is described that indicates the possibility of a non-amino acid biosynthetic pathway in marine natural products.

Graphical abstract: Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B517149K
Article type
Communication
Submitted
05 Dec 2005
Accepted
24 Feb 2006
First published
10 Mar 2006

Chem. Commun., 2006, 1742-1744

Permissions

Request permissions

Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles

T. Ichino, H. Arimoto and D. Uemura, Chem. Commun., 2006, 1742 DOI: 10.1039/B517149K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements