Paper
1,3,4,6-Tetra-O-acetyl-2-chloroacetamido-2-deoxy-beta-D-glucopyranose as a glycosyl donor in syntheses of oligosaccharides.
Published Jul 15, 1990 · F. Dasgupta, L. Anderson
Carbohydrate research
Q2 SJR score
27
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
1,3,4,6-Tetra-O-acetyl-2-chloroacetamido-2-deoxy--d-glucopyranose is a promising glycosyl donor for oligosaccharide synthesis, with good to excellent yields achieved from galacto
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Full text analysis coming soon...
References
Synthesis of a close analog of the repeating unit of the antifreeze glycoproteins of polar fish.
This study successfully synthesized a close analog of the repeating unit of polar fish antifreeze glycoproteins by coupling disaccharide and tripeptide blocks.
1988·24citations·A. Anisuzzaman et al.·Carbohydrate research
Carbohydrate research
Protected glycosides and disaccharides of 2-amino-2-deoxy-D-glucopyranose by ferric chloride-catalyzed coupling.
Ferric chloride-catalyzed glycosylation of hydroxy compounds with protected 2-acylamino-2-deoxy-D-glucopyranose 1-acetates produces protected, -linked disaccharides with 67-80% yields.
1985·59citations·M. Kiso et al.·Carbohydrate research
Carbohydrate research
Lewissäure-katalysierte Synthesen von Di- und Trisaccharid-Sequenzen der O- und N-Glycoproteine. Anwendung von Trimethylsilyltrifluoromethanesulfonat
The study demonstrates the efficient synthesis of di- and trisaccharides using trimethylsilyltrifluoromethanesulfonate as a Lewis acid catalyst, enabling the production of lactosamine and chitobiose derivatives.
1984·117citations·H. Paulsen et al.·Carbohydrate Research
Carbohydrate Research
Synthetic mucin fragments: methyl 3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-β-D-galactopyranoside and methyl 3-O-(2-acetamido-2-deoxy-3-O-β-D-galactopyranosyl-β-D-glucopyranosyl)-β-D-galactopyranoside
This study successfully synthesized and confirmed the structures of various galactopyranoside derivatives, contributing to the understanding of synthetic mucin fragments.
1984·39citations·K. Kohata et al.·Carbohydrate Research
Carbohydrate Research
Synthesis of p-nitrophenyl 2-acetamido-2-deoxy-4-O-β-d-galactopyranosyl- β-d-glucopyranoside, and p-nitrophenyl 6-O-(2-acetamido-2-deoxy-3-O- and -4-O-β-d-galactopyranosyl- β-d-glucopyranosyl)-α-d-mannopyranoside☆
P-nitrophenyl 2-acetamido-2-deoxy-4-O--d-galactopyranosyl- -d-glucopyranoside and p-nitrophenyl 6-O-(2-acetamido-2-deoxy-3-O-
1983·26citations·S. S. Rana et al.·Carbohydrate Research
Carbohydrate Research
A novel, reductive ring-opening of carbohydrate benzylidene acetals☆
Reductive ring-opening of carbohydrate benzylidene acetals using sodium cyanoborohydride-hydrogen chloride is a novel, highly regioselective method for obtaining benzyl groups in products.
1982·350citations·P. Garegg et al.·Carbohydrate Research
Carbohydrate Research
The chemical synthesis of O-α-l-fucopyranosyl-(1→2)-O-β-d-galactopyranosyl-(1→3)-O-[α-l-fucopyranosyl-(1→4)]-2- acetamido-2-deoxy-d-glucopyranose, the lewis b blood-group antigenic determinant
This study developed a rapid synthesis method for the Lewis b blood-group antigenic determinant, enabling the production of the final product in a single step.
1981·24citations·S. S. Rana et al.·Carbohydrate Research
Carbohydrate Research
O-benzylated oxazoline derivatives of 2-acetamido-2-deoxy-d-glucopyranose from 1-propenyl glycosides. synthesis of the propenyl glycosides and their direct cyclization
This study demonstrates a method for synthesizing 1-propenyl glycosides and their conversion into oxazolines, with a modified 0 S 2 conformation for these compounds.
1980·64citations·M. Nashed et al.·Carbohydrate Research
Carbohydrate Research
Citations
Synthesis of lipo-chitooligosaccharide analogues and their interaction with LYR3, a high affinity binding protein for Nod factors and Myc-LCOs.
Lipo-chitooligosaccharide analogues with a triazole unit in the central GlcNAc residue show complete loss of binding to LYR3, a high affinity binding protein for Nod factors and Myc-LCOs.
2017·9citations·Nathan Berthelot et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry
Why Is Direct Glycosylation with N-Acetylglucosamine Donors Such a Poor Reaction and What Can Be Done about It?
Controlling the balance of oxazoline formation and glycosylation is key to achieving acceptable chemical yields in direct glycosylation with N-acetyl-d-glucosamine donors.
2017·17citations·M. Marqvorsen et al.·The Journal of organic chemistry
The Journal of organic chemistry
Biosynthetic and synthetic access to amino sugars.
Recent advances in metal-based catalysts and tethered approaches have significantly improved the synthesis of regio- and stereoselective amino sugars, enabling their use in biomacromolecules and microbial products.
2016·42citations·K. Skarbek et al.·Carbohydrate research
Carbohydrate research
Glycosylation with N-acetyl glycosamine donors using catalytic iron(III) triflate: from microwave batch chemistry to a scalable continuous-flow process
Catalytic iron(III) triflate effectively and selectively glycosylates N-acetyl glycosamine donors, resulting in high yields of simple -glycosides and various linked disaccharides.
2014·19citations·Amandine Xolin et al.·Organic chemistry frontiers
Organic chemistry frontiers
Efficient activation of thioglycosides with N-(p-methylphenylthio)-ε-caprolactam-TMSOTf.
N-(p-methylphenylthio)--caprolactam-TMSOTf effectively activates different thioglycosides for glycosidic bond formation, making it a useful reagent combination for one-pot oligosaccharide assembly strategies.
2012·18citations·S. Maity et al.·Carbohydrate research
Carbohydrate research