Issue 5, 2003
From the journal:

Organic & Biomolecular Chemistry

A convenient route to the furopyran core of dysiherbaine

Okiko Miyata,a   Ryuichi Iba,a   Jun Hashimotoa  and  Takeaki Naito*a  

* Corresponding authors

a Kobe Pharmaceutical University, Motoyamakita, Kobe 658-8558, Japan
E-mail: taknaito@kobepharma-u.ac.jp

Abstract

The bicyclic core, furo[3,2-b]pyran, of the dysiherbaines has been synthesized via two routes involving the imino 1,2-Wittig rearrangement of allyl furohydroximate and the asymmetric dihydroxylation of furylpropenol derivative.

Graphical abstract: A convenient route to the furopyran core of dysiherbaine

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Article information

DOI
https://doi.org/10.1039/B212556K
Article type
Communication
Submitted
21 Dec 2002
Accepted
30 Jan 2003
First published
10 Feb 2003

Org. Biomol. Chem., 2003,1, 772-774

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A convenient route to the furopyran core of dysiherbaine

O. Miyata, R. Iba, J. Hashimoto and T. Naito, Org. Biomol. Chem., 2003, 1, 772 DOI: 10.1039/B212556K

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