Chiral 2-C-methylene glycosides and carbohydrate-derived pyrano[2,3-b][1]benzopyrans: synthesis via InCl3 catalyzed stereoselective Ferrier rearrangement of 2-C-acetoxymethyl glycal derivatives-Reference-Cited by-同舟云学术

Chiral 2-C-methylene glycosides and carbohydrate-derived pyrano[2,3-b][1]benzopyrans: synthesis via InCl3 catalyzed stereoselective Ferrier rearrangement of 2-C-acetoxymethyl glycal derivatives

Published:2005-11 Issue:46 Volume:46 Page:8047-8051
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ghosh Rina,Chakraborty Arijit,Maiti Dilip K.,Puranik Vedavati G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference37 articles.

1. Branched-chain 2-deoxy sugars. V. Application of the Wittig reaction to methyl 3,4-O-isopropylidene-β-D-erythro-pentopyranosid-2-ulose and attempted synthesis of nucleosides of 2-deoxy-2-C-methylpentoses

2. Preparation of analogues of the carbohydrate moiety of the polyoxins

3. Synthesis of fused lactone nucleosides via stereoselective Wittig olefination of hexopyranosyl keto-nucleosides

4. A Convenient Route for the Synthesis of 2-C-Substituted 2-Deoxyhexoses

5. Synthesis and Antiviral Activities of 5-Substituted 1-(2-Deoxy-2-C-methylene-4-thio-β-D-erythro-pentofuranosyl)uracilst

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