Issue 6, 2005
From the journal:

Natural Product Reports

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

Tsion Bililign,a   Byron R. Griffithbc  and  Jon S. Thorson*bc  

* 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

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B407364A
Article type
Review Article
Submitted
28 Jul 2005
First published
28 Sep 2005

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

Permissions

Request permissions

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

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