Regioselective Synthesis of Vinylic Derivatives of Common Monosccarides Through Their Activated Stannylene Acetal Intermediates-Reference-Cited by-同舟云学术

Regioselective Synthesis of Vinylic Derivatives of Common Monosccarides Through Their Activated Stannylene Acetal Intermediates

Published:2005-08-31 Issue:7 Volume:10 Page:772-782
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Namazi H.,Sharifzadeh R.

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/10/7/772/pdf

Reference22 articles.

1. Stannylene acetal-mediated regioselective open glycosylation of methyl β-d-galactopyranoside and methyl α-l-rhamnopyranoside

2. Regioselective acylation of secondary hydroxyl groups in sugars catalyzed by lipases in organic solvents

3. On the selectivity of stannylene-mediated alkylation and esterification of methyl 4,6-O-benzylidene α-d-glucopyranoside

4. Biocatalytic synthesis of sugar-containing polyacrylate-based hydrogels

5. 4,6-O-Benzylidene-d-glucopyranose and its sodium salt: new data on their preparation and properties

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