Chapter 29. Anhydrohexitols as Conformationally Constrained Furanose Mimics, Design of an RNA-Receptor
- Yves Chapleur
Published Online: 28 JAN 2005
DOI: 10.1002/3527603239.ch29
Copyright © 1998 Wiley-VCH Verlag GmbH
Book Title
Carbohydrate Mimics: Concepts and Methods
Additional Information
How to Cite
Herdewijn, P. (2005) Anhydrohexitols as Conformationally Constrained Furanose Mimics, Design of an RNA-Receptor, in Carbohydrate Mimics: Concepts and Methods (ed Y. Chapleur), Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, FRG. doi: 10.1002/3527603239.ch29
Editor Information
UMR CNRS 7565, Université Henri Poincaré-Nancy I, BP239, F-54506 Vandceuvre, France
Publication History
- Published Online: 28 JAN 2005
- Published Print: 12 NOV 1997
ISBN Information
Print ISBN: 9783527295265
Online ISBN: 9783527603237
- Summary
- Chapter
Keywords:
- anhydrohexitols;
- furanose;
- RNA-receptor;
- oligonucleotides;
- 2′,3′-dideoxy-3′-C-hydroxymethyl-α-l-threo-pentopyranosyl nucleoside;
- 1,5-anhydro-2,3-dideoxy-d-arabino-hexitol nucleoside;
- six-membered carbohydrate-like moiety
Summary
Introduction
Double Stranded RNA Structure
Design of Oligonucleotides with a Six Membered Carbohydrate Moiety
Synthesis of 2′,3′-Dideoxy-3′-C-Hydroxymethyl-α-l-threo-Pentopyranosyl Nucleoside and 1,5-Anhydro-2,3-Dideoxy-d-arabino-Hexitol Nucleoside
Oligonucleotide Built up from Nucleosides with a Six-membered Carbohydrate-like Moiety
1,5-Anhydrohexitol Nucleoside as a Mimic of a Furanose Nucleoside in its 2′-endo/3′-exo Conformation
References