The Wittig-cyclization procedure: acid promoted intramolecular formation of 3-C-branched-chain 3,6-anhydro furano sugars via 2′-oxopropylene derivatives-Reference-Cited by-同舟云学术

The Wittig-cyclization procedure: acid promoted intramolecular formation of 3-C-branched-chain 3,6-anhydro furano sugars via 2′-oxopropylene derivatives

Published:2007-06 Issue:8 Volume:342 Page:1091-1095
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Ay Kadir,Çetin Fatma,Yüceer Levent

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference25 articles.

1. Synthesis and Reactions of 3-C-Branched-Chain Analogues of 3,6-Anhydrodeoxynojirimycin

2. C-Glycosyl nucleosides. V. Unexpected observations on the relative stabilities of compounds containing fused five-membered rings with epimerizable substituents

3. Stereospecific synthesis of ethyl (2-acetamido-2-deoxy-α-d-glucopyranosyl)-acetate

4. Wittig reaction with partially protected sugar lactol derivatives. Preparation of highly cytotoxic goniofufurone analogues

5. Diastereoselektive synthese von funktionalisierten C-α- und -β-glykosylderivaten der 2-acetamido-2-desoxy-d-glucose

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