Synthesis of curdlan derivatives regioselectively modified at C-6: O-(N)-Acylated 6-amino-6-deoxycurdlan-Reference-Cited by-同舟云学术

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Synthesis of curdlan derivatives regioselectively modified at C-6: O-(N)-Acylated 6-amino-6-deoxycurdlan

Published:2014-05 Issue: Volume:105 Page:161-168
ISSN:0144-8617
Container-title:Carbohydrate Polymers
language:en
Short-container-title:Carbohydrate Polymers

Author:

Zhang Ruoran,Edgar Kevin J.

Funder

Institute for Critical Technologies and Applied Science (ICTAS)

Macromolecules and Interfaces Institute (MII) at Virginia Tech

National Science Foundation

Publisher

Elsevier BV

Subject

Materials Chemistry,Polymers and Plastics,Organic Chemistry

Reference38 articles.

1. Cyclodextrin chemistry. Selective modification of all primary hydroxyl groups of α- and β-cyclodextrins;Boger;Helvetica Chimica Acta,1978

2. Synthesis and anti-HIV activity of -6-amino-6-deoxy-(1→3)-β-d-curdlan sulfate;Borjihan;Polymers for Advanced Technologies,2003

3. Chitosan nanoparticles for oral drug and gene delivery;Bowman;International Journal of Nanomedicine,2006

4. Plasmodium falciparum domain mediating adhesion to chondroitin sulfate A: A receptor for human placental infection;Buffet;Proceedings of the National Academy of Sciences of the United States of America,1999

5. A direct regioselective route to 6-azido-6-deoxy polysaccharides under mild and homogeneous conditions;Cimecioglu;Macromolecules,1997

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