Issue 13, 1999
From the journal:

Chemical Communications

An extremely mild and stereocontrolled construction of 1,2-cis-α-glycosidic linkages via benzyl-protected glycopyranosyl diethyl phosphites

Hiroko Tanaka,   Hiroki Sakamoto,   Ai Sano,   Seiichi Nakamura,   Makoto Nakajima  and  Shunichi Hashimoto  

Abstract

A highly stereocontrolled 1,2-cis-α-glycosidation reaction under conditions mild enough for acid-labile alcohols has been developed using benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors in the presence of 2,6-di-tert-butylpyridinium iodide and tetrabutylammonium iodide.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/A902845E
Article type
Paper

Chem. Commun., 1999, 1259-1260

Permissions

Request permissions

An extremely mild and stereocontrolled construction of 1,2-cis-α-glycosidic linkages via benzyl-protected glycopyranosyl diethyl phosphites

H. Tanaka, H. Sakamoto, A. Sano, S. Nakamura, M. Nakajima and S. Hashimoto, Chem. Commun., 1999, 1259 DOI: 10.1039/A902845E

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