Issue 38, 2009
From the journal:

Chemical Communications

Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations†

Huimin Zhai,a   Maria Zlotorzynskaa  and  Glenn Sammis*a  

* Corresponding authors

a Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada
E-mail: gsammis@chem.ubc.ca

Abstract

Nitrogen-centered radical cyclizations onto silyl enol ethers were utilized for the syntheses of protected polyhydroxylated pyrrolidines 2-hydroxymethyl-3-hydroxypyrrolidine and 1,4-dideoxy-1,4-imino-L-ribitol.

Graphical abstract: Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations

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Article information

DOI
https://doi.org/10.1039/B914757H
Article type
Communication
Submitted
22 Jul 2009
Accepted
10 Aug 2009
First published
02 Sep 2009

Chem. Commun., 2009, 5716-5718

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Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations

H. Zhai, M. Zlotorzynska and G. Sammis, Chem. Commun., 2009, 5716 DOI: 10.1039/B914757H

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