Issue 38, 2011

Reverse orthogonal strategy for oligosaccharide synthesis§

Abstract

Herein, we report the invention of a novel expeditious concept for oligosaccharide synthesis. Unlike the classic orthogonal strategy based on leaving groups, the reverse approach is based on orthogonal protecting groups, herein p-methoxybenzyl and 4-pentenoyl, which allows for efficient oligosaccharide assembly in the reverse direction.

Graphical abstract: Reverse orthogonal strategy for oligosaccharide synthesis

Supplementary files

Article information

Article type
Communication
Submitted
09 Мау. 2011
Accepted
16 Там. 2011
First published
05 Қыр. 2011

Chem. Commun., 2011,47, 10602-10604

Reverse orthogonal strategy for oligosaccharide synthesis

K. Fujikawa, N. V. Ganesh, Y. H. Tan, K. J. Stine and A. V. Demchenko, Chem. Commun., 2011, 47, 10602 DOI: 10.1039/C1CC13409D

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