Results 211 to 220 of about 54,595 (236)
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Glycosylation using glycosyl phosphite as a glycosyl donor
Tetrahedron, 1994Abstract Glycosylation using glycosyl phosphites as glycosyl donors in the presence of a Lewis acid such as ZnCl2 or ZnCl2-AgClO4 has afforded the glycosides including sialoglycosides in good yields.
Yutaka Watanabe +3 more
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Stereoselective glycosylation using oxathiane glycosyl donors
Chemical Communications, 2009A bicyclic glycosyl donor is activated as an arylsulfonium ion and used to synthesise alpha-glycosides with high stereoselectivity.
Fascione, Martin A. +5 more
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Current Opinion in Structural Biology, 2019
Despite the ubiquity of collagens in the animal kingdom, little is known about the biology of the disaccharide Glc(α1-2)Gal(β1-O) bound to hydroxylysine across collagens from sponges to mammals. The extent of collagen glycosylation varies by the types of collagen, with basement membrane collagen type IV being more glycosylated than fibrillar collagens.
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Despite the ubiquity of collagens in the animal kingdom, little is known about the biology of the disaccharide Glc(α1-2)Gal(β1-O) bound to hydroxylysine across collagens from sponges to mammals. The extent of collagen glycosylation varies by the types of collagen, with basement membrane collagen type IV being more glycosylated than fibrillar collagens.
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Artificial Glycosyl Phosphorylases
Chemistry – A European Journal, 2005Abstractα‐ and β‐Cyclodextrin 6A,6D‐diacids (1 and 2), β‐cyclodextrin‐6‐monoacid (14), β‐cyclodextrin 6A,6D‐di‐O‐sulfate (16) and β‐cyclodextrin‐6‐heptasulfate (19) were synthesised. Acids 1, 2 and 14 were made from perbenzylated α‐ or β‐cyclodextrin, by diisobutylaluminum hydride (DIBAL)‐promoted debenzylation, oxidation and deprotection.
Rousseau, C. +5 more
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Glycosylation of alcohols using glycosyl boranophosphates as glycosyl donors
Tetrahedron Letters, 2013Abstract A novel glycosylation that uses glycosyl boranophosphate triesters as glycosyl donors and trityl cation (Tr+) as an activator was developed. Two types of reactions were studied: (1) the boranophosphate triester was activated with TrNTf2 to react with an alcohol and (2) O-trityl ethers worked as both glycosyl acceptors and Tr+ sources.
Shiro Tatsumi +3 more
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N-Glycosyl Amides as Glycosyl Donors in Stereoselective Glycosylation Reactions
Synthesis, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
Norbert Pleuss, Horst Kunz
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Glycosyl hydrolase catalyzed glycosylation in unconventional media
Applied Microbiology and Biotechnology, 2020The reversible hydrolytic property of glycosyl hydrolases (GHs) as well as their acceptance of aglycones other than water has provided the abilities of GHs in synthesizing glycosides. Together with desirable physiochemical properties of glycosides and their high commercial values, research interests have been aroused to investigate the synthetic other ...
Hanchi Chen +6 more
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Carbohydrate Research, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Mårten, Jacobsson +2 more
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Mårten, Jacobsson +2 more
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Highly α‐Selective Glycosylation with Glycosyl Acetate via Glycosyl Phosphonium Iodide.
ChemInform, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
Yohei Kobashi, Teruaki Mukaiyama
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Glycosylation with N-Troc-protected glycosyl donors
Carbohydrate Research, 1996N-Troc-protected (Troc = 2,2,2-trichloroethoxycarbonyl) glucosamine and galactosamine glycosyl donors (1-O-acetyl sugar, bromo sugar, and thioglycoside) were compared with the corresponding N-Phth-protected derivatives in glycosylations of 2-(trimethylsilyl)ethanol, 2-bromoethanol, methyl 3-mercaptopropionate, N-Fmoc-protected serine, and 2 ...
U, Ellervik, G, Magnusson
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