Scope and limitation of the application of the (methoxydimethyl)methyl group in the synthesis of 2′-O-, 6′-O- and 2′,6′-di-O-(α-l-arabinofuranosyl)-β-d-galactopyranosyl-(1→6)-d-galactoses
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference23 articles.
1. Structural analysis of a 4-O-methyl-glucuronoarabinoxylan with immuno-stimulating activity from Echinacea purpurea
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3. One-pot synthesis of branched oligosaccharides by use of galacto- and mannopyranosyl thioglycoside diols as key glycosylating agents;Organic & Biomolecular Chemistry;2013
4. Selective removal of the (2-naphthyl)methyl protecting group in the presence of p-methoxybenzyl group by catalytic hydrogenation;Arkivoc;2012-06-22
5. ChemInform Abstract: Scope and Limitation of the Application of the (Methoxydimethyl)methyl Group in the Synthesis of 2′-O-, 6′-O- and 2′,6′-Di-O-(α-L-arabinofuranosyl)-β-D-galactopyranosyl- (1→6)-D-galactoses.;ChemInform;2010-06-12
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