Paper
Facile synthesis of 2-methyl-[4,6-di-O-acetyl-1,2-dideoxy-3-O-(2,3,4,6-tetra-O-acetyl-D-glycopyranosyl)-alpha-D-glucopyrano-[2',1':4,5]-2-oxazolines, key intermediates for the synthesis of oligosaccharides.
Published 1977 · K. Matta, J. Barlow
Carbohydrate research
Q2 SJR score
17
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
This study developed a simple synthesis method for disaccharide oxazolines, which are key intermediates in the synthesis of oligosaccharides.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
A facile synthesis of 2-methyl-[3,4-di-O-acetyl-6-O-(chloroacetyl)-1,2-dideoxy-alpha-D-glucopyrano]-[2',1':4,5]-2-oxazoline.
The chloroacetyl group can be effectively used as a protecting group in the synthesis of 2-methylglyco-[2',1':4,5]-2-oxazoline, with selective removal possible using thiourea.
1976·17citations·K. Matta et al.·Carbohydrate research
Carbohydrate research
Synthesis of 1-thioaldosides having an amino group at the aglycon terminal
1-thioaldosides with an amino group at the aglycon terminal were successfully synthesized from acetylated 1-halides of d-galactose, d-glucose, and 2-amino-2-deoxy-d-glucose.
1973·79citations·Stefan Chipowsky et al.·Carbohydrate Research
Carbohydrate Research
The synthesis of O-α-d-mannopyranosyl-(1→6)-O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1→4)-2-acetamido-2-deoxy-d-glucose
This study synthesized a trisaccharide that serves as a reference compound for determining the structure of glycopeptides and as a starting material for their synthesis.
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Carbohydrate Research
Oxazoline synthesis of 1,2-trans-2-acetamido-2-deoxyglycosides. Glycosylation of secondary hydroxyl groups in partially protected saccharides
The oxazoline method effectively synthesizes 1,2-trans-2-acetamido-2-deoxyglycosides, enabling the synthesis of various glycosylated partially protected saccharides with free secondary hydroxyl groups.
1970·42citations·S. E. Zurabyan et al.·Carbohydrate Research
Carbohydrate Research
Synthesis of various glycosides of 2-amino-3-O-D-1-carboxyethyl)-2-deoxy-D-glucopyranose (muramic acid)
This study demonstrates the synthesis of various glycosides of 2-amino-3-O-D-1-carboxyethyl)-2-deoxy-D-glucopyranose (muramic acid) with high yields and resistance to egg-white lysozyme action.
1968·34citations·R. Jeanloz et al.·Carbohydrate Research
Carbohydrate Research
CONFIGURATION OF GLYCOSIDIC LINKAGES IN OLIGOSACCHARIDES: IX. SYNTHESIS OF α- AND β-D-MANNOPYRANOSYL DISACCHARIDES
The Konigs-Knorr method can synthesize 6-O--D-mannopyranosyl-D-glucose, a metabolite produced by Ustilago species, and its -D-linked isomer.
1961·99citations·P. Gorin et al.·Canadian Journal of Chemistry
Canadian Journal of Chemistry
Citations
A Facile Method for Synthesis of 1,2-Oxazoline Derivative of N-Acetylglucosamine Promoted by Potassium Fluoride
Potassium fluoride-promoted intramolecular cyclization of 2-acetamido-2-deoxy--D-glucopyranosyl chloride effectively synthesizes 1,2-oxazoline derivatives with simple experimental procedures.
2002·8citations·S. Shoda et al.·Chemistry Letters
Chemistry Letters
A facile synthesis of 2-acetamido-2-deoxy-4-O-α-l-fucopyranosyl-3-O-β-d-galactopyranosyl-d-glucopyranose, the Lewis a blood-group antigenic determinant, and related compounds
This study developed a simple strategy for synthesis of 2-acetamido-2-deoxy-4-O--l-fucopyranosyl-3-O--d-galactopyranosyl-d-glucopyranose, the Lewis a blood-group anti
1983·11citations·S. S. Rana 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
Synthesis of phenyl 2-acetamido-2-deoxy-3-O-α-l-fucopyranosyl-β-d-glucopyranoside and related compounds
Phenyl 2-acetamido-2-deoxy-3-O--l-fucopyranosyl--d-glucopyranoside and related compounds can be synthesized using halide ion-catalyzed conditions.
1981·7citations·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
Synthesis of glycolipids.
This paper reviews the chemical syntheses of various naturally occurring glycolipids and lipid intermediates, providing insights into their synthesis methods up to 1977.
1980·62citations·R. Gigg·Chemistry and physics of lipids
Chemistry and physics of lipids
The synthesis ofP1-[2-acetamido-2-deoxy-3-O-(β-D-glucopyranosyluronic acid)-α-D-glucopyranosyl] P2-dolichyl diphosphate (N-acetylhyalobiosyluronic dolichyl diphosphate)
The study successfully synthesized N-acetyl-hyalobiosyluronic dolichyl diphosphate from 2-acetamido-4,6-di-O-acetyl-2-deoxy-3-O-(-D-glucopyranosyl
1979·10citations·E. Walker‐Nasir et al.·Carbohydrate Research
Carbohydrate Research
Action of endo-alpha-N-acetyl-D-galactosaminidase on synthetic glycosides including chromogenic substrates.
Endo-alpha-N-acetyl-D-galactosaminidase effectively cleaves synthetic glycosides, revealing its specificity for Gal--GalNAc linked via an -linkage, and can be used as an affinity ligand for purification of the
1978·21citations·J. Umemoto et al.·Analytical biochemistry
Analytical biochemistry