Structure, activity, synthesis and biosynthesis of aryl-C-glycosides (original) (raw)

Author affiliations

* Corresponding authors

a Johns Hopkins University, Chemistry Department, 3400 North Charles Street, Baltimore, MD
E-mail: tbilili1@jhu.edu

b University of Wisconsin, School of Pharmacy, Laboratory for Biosynthetic Chemistry, 777 Highland Avenue, Madison, WI
E-mail: brgriffith@pharmacy.wisc.edu, jsthorson@pharmacy.wisc.edu

c University of Wisconsin National Cooperative Drug Discovery Group

Abstract

Covering: the literature up to April 2005

The focus of this review is to highlight the structure, bioactivity and biosynthesis of naturally occurring aryl-_C_-glycosides. General synthetic methods and their relevance to proposed biochemical mechanisms for the aryl-_C_-glycoside bond formation are also presented.

Graphical abstract: Structure, activity, synthesis and biosynthesis of aryl-C-glycosides

You have access to this article

Please wait while we load your content... Something went wrong. Try again?

Article information

DOI

https://doi.org/10.1039/B407364A

Article type

Review Article

Submitted

28 Jul 2005

First published

28 Sep 2005

Download Citation

Nat. Prod. Rep., 2005,22, 742-760

Permissions

Structure, activity, synthesis and biosynthesis of aryl-_C_-glycosides

T. Bililign, B. R. Griffith and J. S. Thorson,Nat. Prod. Rep., 2005, 22, 742DOI: 10.1039/B407364A

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