Issue 38, 2009

Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations

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

Supplementary files

Article information

Article type
Communication
Submitted
22 Jul 2009
Accepted
10 Aug 2009
First published
02 Sep 2009

Chem. Commun., 2009, 5716-5718

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements