Issue 34, 2011
From the journal:

Chemical Communications

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

Shino Manabe,*a   Yoshiyuki Aiharaa  and  Yukishige Itoab  

* Corresponding authors

a RIKEN, Advanced Science Institute, Hirosawa, Wako-shi, Saitama, Japan
E-mail: smanabe@riken.jp
Fax: +81 48 462 4680
Tel: +81 48 467 9432

b ERATO, JST, Hirosawa, Wako-shi, Saitama, Japan

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

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1CC13172A
Article type
Communication
Submitted
30 မေ 2011
Accepted
11 ဇူ 2011
First published
25 ဇူ 2011

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

Permissions

Request permissions

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