Issue 22, 2015

A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B

Abstract

An efficient and high-yielding synthesis of penaresidin B is disclosed herein. The concise 8-step synthesis of azetidine aldehyde was devised by incorporating our novel strategy for ready access to 3-amino-2,3-dideoxysugars via regio- and stereoselective tandem hydroamination/glycosylation of glycal as the key step.

Graphical abstract: A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B

Supplementary files

Article information

Article type
Communication
Submitted
11 Dec 2014
Accepted
07 Feb 2015
First published
18 Feb 2015
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2015,51, 4639-4642

A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B

F. Ding, R. William, S. M. Kock, M. L. Leow and X. Liu, Chem. Commun., 2015, 51, 4639 DOI: 10.1039/C4CC09904D

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