Inter vs. intraglycosidic acetal linkages control sulfation pattern in semi-synthetic chondroitin sulfate-Reference-Cited by-同舟云学术

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Inter vs. intraglycosidic acetal linkages control sulfation pattern in semi-synthetic chondroitin sulfate

Published:2014-11 Issue: Volume:112 Page:546-555
ISSN:0144-8617
Container-title:Carbohydrate Polymers
language:en
Short-container-title:Carbohydrate Polymers

Author:

Laezza Antonio,De Castro Cristina,Parrilli Michelangelo,Bedini Emiliano

Funder

Ministero dell’Istruzione dell’Università e della Ricerca (MIUR)

Publisher

Elsevier BV

Subject

Materials Chemistry,Polymers and Plastics,Organic Chemistry

Reference47 articles.

1. Facile cleavage of carbohydrate benzyl ethers and benzylidene acetals using the NaBrO3/Na2S2O4 reagent under two-phase conditions;Adinolfi;Tetrahedron Letters,1999

2. The acetonation of lactose and benzyl β-lactoside with 2-methoxypropene;Alonso-Lopez;Tetrahedron,1987

3. Acetal-derivatized dextran: An acid-responsive biodegradable material for therapeutic applications;Bachelder;Journal of the American Chemical Society,2008

4. Improved preparation of 2,3:5,6:3′,4′-tri-O-isopropylidenelactose dimethyl acetal and its 6′-O-(1-methoxy-1-methylethyl) derivative;Barili;Carbohydrate Research,1997

5. A microbiological–chemical strategy to produce chondroitin sulfate A,C;Bedini;Angewandte Chemie International Edition,2011

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