Direct synthesis of β-d-Xyl-(1→2)-β-d-Man-(1→4)-α-d-Glc-OME: a trisaccharide component of the Hyriopsis schlegelii glycosphingolipid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Formation of β-Mannopyranosides of Primary Alcohols Using the Sulfoxide Method
2. Direct Synthesis of β-Mannopyranosides by the Sulfoxide Method
3. Glycosylation of unreactive substrates
4. Generalizing Glycosylation: Synthesis of the Blood Group Antigens Lea, Leb, and Lex Using a Standard Set of Reaction Conditions
5. Are Glycosyl Triflates Intermediates in the Sulfoxide Glycosylation Method? A Chemical and 1H, 13C, and 19F NMR Spectroscopic Investigation
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1. Glycosyl Sulfoxides in Glycosylation Reactions;Topics in Current Chemistry;2018-06-12
2. Stereoselective β-mannosylation via anomeric O-Alkylation: Concise synthesis of β-D-Xyl-(l→2)-β-D-Man-(1→4)-α-D-Glc-OMe, a trisaccharide oligomer of the hyriopsis schlegelii glycosphingolipid;Journal of Carbohydrate Chemistry;2017-06-13
3. A unique approach to the synthesis of a dengue vaccine and the novel tetrasaccharide that results;Tetrahedron: Asymmetry;2009-05
4. Oligosaccharide Synthesis;Carbohydrates: The Essential Molecules of Life;2009
5. Stereoselective Synthesis of β-manno-Glycosides;Glycoscience;2008
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