Issue 16, 2020

C-Glycosylation enabled by N-(glycosyloxy)acetamides

Abstract

The C-glycosylation of C-nucleophiles including allyltrimethylsilane, silyl enol ethers and phenols with N-(glycosyloxy)acetamides as glycosyl donors has been realized. This protocol provides a convenient and practical route for the synthesis of alkyl C-glycosides and aryl 2-deoxy-β-C-glycosides under mild reaction conditions.

Graphical abstract: C-Glycosylation enabled by N-(glycosyloxy)acetamides

Supplementary files

Article information

Article type
Communication
Submitted
17 Kul 2020
Accepted
30 Kul 2020
First published
31 Kul 2020

Org. Biomol. Chem., 2020,18, 3043-3046

C-Glycosylation enabled by N-(glycosyloxy)acetamides

M. Liu, B. Li, T. Li, X. Wu, M. Liu, D. Xiong and X. Ye, Org. Biomol. Chem., 2020, 18, 3043 DOI: 10.1039/D0OB00561D

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