Issue 22, 2006
From the journal:

Chemical Communications

Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis†

Kevin B. Bahncka  and  Scott D. Rychnovsky*a  

* Corresponding authors

a Department of Chemistry, 1102 Natural Sciences II, University of California, Irvine, Irvine, CA, USA
E-mail: srychnov@uci.edu
Fax: +1 949-824-6379
Tel: +1 949-824-8292

Abstract

Prins cyclization using an electron-rich benzaldehyde and a homoallylic alcohol efficiently delivered the fully substituted C-aryl tetrahydropyranoside of kendomycin.

Graphical abstract: Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis

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Article information

DOI
https://doi.org/10.1039/B602937J
Article type
Communication
Submitted
25 Feb 2006
Accepted
30 Mar 2006
First published
02 May 2006

Chem. Commun., 2006, 2388-2390

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Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis

K. B. Bahnck and S. D. Rychnovsky, Chem. Commun., 2006, 2388 DOI: 10.1039/B602937J

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