Issue 10, 2004
From the journal:

Chemical Communications

Synthetic approach to kendomycin: preparation of the C-glycosidic core†

Tetsuya Sengoku,a   Hirokazu Arimoto*ab  and  Daisuke Uemuraa  

* Corresponding authors

a Department of Chemistry, Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan
E-mail: arimoto@org.chem.nagoya-u.ac.jp
Fax: +81 52 789 5041
Tel: +81 52 789 2480

b Institute for Advanced Research, Nagoya University; and PRESTO, JST, Chikusa, Nagoya 464-8602, Japan

Abstract

Synthesis of the C13–C19 C-glycoside portion of kendomycin was achieved via oxidative pyran cyclization and Claisen rearrangement to construct the fully functionalized aromatic ring.

Graphical abstract: Synthetic approach to kendomycin: preparation of the C-glycosidic core

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Article information

DOI
https://doi.org/10.1039/B402391A
Article type
Communication
Submitted
17 Feb 2004
Accepted
22 Mar 2004
First published
23 Apr 2004

Chem. Commun., 2004, 1220-1221

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Synthetic approach to kendomycin: preparation of the C-glycosidic core

T. Sengoku, H. Arimoto and D. Uemura, Chem. Commun., 2004, 1220 DOI: 10.1039/B402391A

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