Synthesis of an arabinogalactan-type octa- and two isomeric nonasaccharides. Suitable tuning of protecting groups
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
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1. One-pot synthesis of a 3,6-branched hexaarabinogalactan using galactopyranosyl thioglycoside diol as a key glycosylating agent;Journal of Asian Natural Products Research;2014-05-30
2. Selective Deprotection Method of N-Phenylcarbamoyl Group;The Journal of Organic Chemistry;2013-08-13
3. One-pot synthesis of branched oligosaccharides by use of galacto- and mannopyranosyl thioglycoside diols as key glycosylating agents;Organic & Biomolecular Chemistry;2013
4. Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies;Carbohydrate Research;2009-08
5. Synthesis of plant arabinogalactans;Frontiers of Chemistry in China;2009-02-03
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