Issue 34, 2011

Radical C-glycosylation reaction of pyranosides with the 2,3-trans carbamate group

Abstract

Radical-mediated C-glycosylation of pyranosides with the 2,3-trans carbamate group was investigated. C-Glycosylation was achieved with high α-selectivity.

Graphical abstract: Radical C-glycosylation reaction of pyranosides with the 2,3-trans carbamate group

Supplementary files

Article information

Article type
Communication
Submitted
30 Мам. 2011
Accepted
11 Шіл. 2011
First published
25 Шіл. 2011

Chem. Commun., 2011,47, 9720-9722

Radical C-glycosylation reaction of pyranosides with the 2,3-trans carbamate group

S. Manabe, Y. Aihara and Y. Ito, Chem. Commun., 2011, 47, 9720 DOI: 10.1039/C1CC13172A

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