Issue 96, 2016, Issue in Progress

Stereoselective glycoconjugation of steroids with selenocarbohydrates

Abstract

A methodology that brings together sugar and steroid scaffolds linked by a selenium atom is discussed in this work. A series of 6β and 3α glycoconjugated steroids were achieved by stereoselective nucleophilic substitution of cholesterol, pregnenolone, stigmasterol and sitosterol with different seleno-pyranosides and furanosides.

Graphical abstract: Stereoselective glycoconjugation of steroids with selenocarbohydrates

Supplementary files

Article information

Article type
Paper
Submitted
26 Aug 2016
Accepted
24 Sep 2016
First published
26 Sep 2016

RSC Adv., 2016,6, 93905-93914

Stereoselective glycoconjugation of steroids with selenocarbohydrates

R. F. Affeldt, F. P. Santos, R. S. da Silva, O. E. D. Rodrigues, L. A. Wessjohann and D. S. Lüdtke, RSC Adv., 2016, 6, 93905 DOI: 10.1039/C6RA21485A

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