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

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Article information

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

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

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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

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