Synthesis of hexasaccharide fragment of lipoarabonomannan from Mycobacteria: advantages of the benzyl-free approach
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Title
Synthesis of hexasaccharide fragment of lipoarabonomannan from Mycobacteria: advantages of the benzyl-free approach
Authors
Keywords
arabinofuranose, lipoarabinomannan, benzyl-free approach, 1,2-<em class=EmphasisTypeItalic >cis</em>-glycosylation
Journal
RUSSIAN CHEMICAL BULLETIN
Volume 64, Issue 5, Pages 1149-1162
Publisher
Springer Nature
Online
2016-01-29
DOI
10.1007/s11172-015-0992-5
References
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- Probing the Effect of Acylation on Arabinofuranose Ring Conformation in Di- and Trisaccharide Fragments of Mycobacterial Arabinogalactan
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- β-Selective Arabinofuranosylation Using a 2,3-O-Xylylene-Protected Donor
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- (2009) Vu Hong et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Copper-Free Azide–Alkyne Cycloadditions: New Insights and Perspectives
- (2008) Jean-François Lutz ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Cu-Catalyzed Azide−Alkyne Cycloaddition
- (2008) Morten Meldal et al. CHEMICAL REVIEWS
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