Results 261 to 270 of about 15,326,315 (274)
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Chemical Communications, 2014
Combining triflic acid-catalyzed acetalation, benzylation, reductive ring opening of benzylidene acetal and glycosylation in one-pot transformations leads to a wide range of d-glucosamine building blocks for assembling oligomers.
G. Despras+3 more
semanticscholar +1 more source
Combining triflic acid-catalyzed acetalation, benzylation, reductive ring opening of benzylidene acetal and glycosylation in one-pot transformations leads to a wide range of d-glucosamine building blocks for assembling oligomers.
G. Despras+3 more
semanticscholar +1 more source
, 2014
D-Glucosamine is reported for the first time as a green ligand for copper catalyzed coupling of aryl halides and sodium sulfinates, which provides a simple and extremely efficient new route to unsymmetrical diaryl sulfones.
Ming‐Ming Yang+4 more
semanticscholar +1 more source
D-Glucosamine is reported for the first time as a green ligand for copper catalyzed coupling of aryl halides and sodium sulfinates, which provides a simple and extremely efficient new route to unsymmetrical diaryl sulfones.
Ming‐Ming Yang+4 more
semanticscholar +1 more source
Chemistry, 2015
Cyclo-oligo-(1→6)-β-D-glucosamines functionalized with hydrophobic tails are reported as a new class of transmembrane ion-transport system. These macrocycles with hydrophilic cavities were introduced as an alternative to cyclodextrins, which are ...
Arundhati Roy+7 more
semanticscholar +1 more source
Cyclo-oligo-(1→6)-β-D-glucosamines functionalized with hydrophobic tails are reported as a new class of transmembrane ion-transport system. These macrocycles with hydrophilic cavities were introduced as an alternative to cyclodextrins, which are ...
Arundhati Roy+7 more
semanticscholar +1 more source
Chemical Communications, 2014
Unimolecular ion channels were designed by functionalization of a new type of cyclic oligosaccharides, cyclo-oligo-(1 → 6)-β-d-glucosamines, with pentabutylene glycol chains. Their ion transporting activity was tuned by varying oligomericity.
T. Saha+7 more
semanticscholar +1 more source
Unimolecular ion channels were designed by functionalization of a new type of cyclic oligosaccharides, cyclo-oligo-(1 → 6)-β-d-glucosamines, with pentabutylene glycol chains. Their ion transporting activity was tuned by varying oligomericity.
T. Saha+7 more
semanticscholar +1 more source
Synthesis of oseltamivir and tamiphosphor from N-acetyl-D-glucosamine.
Organic and biomolecular chemistry, 2013Using N-acetyl-D-glucosamine as a starting material, the anti-influenza drugs oseltamivir and tamiphosphor were synthesized via a pivotal intermediate of aldehyde 8.
Chih-An Chen, Jim-Min Fang
semanticscholar +1 more source
Optical turn-on sensor based on graphene oxide for selective detection of D-glucosamine.
Analytical Chemistry, 2012By incorporating the well-known fluorophore 8-aminoquinoline into graphene oxide, we have successfully prepared a turn-on fluorescent sensor capable of specific detection of D-glucosamine with a high selectivity and sensitivity. This methodology provides
Rumei Cheng+7 more
semanticscholar +1 more source
Non-catalytic synthesis of Chromogen I and III from N-acetyl-D-glucosamine in high-temperature water
, 2013Non-catalytic synthesis of 2-acetamido-2,3-dideoxy-D-erythro-hex-2-enofuranose (Chromogen I) and 3-acetamido-5-(1′,2′-dihydroxyethyl)furan (Chromogen III) from N-acetyl-D-glucosamine (GlcNAc) was achieved, with the highest yields of 23.0% and 23.1 ...
M. Osada+5 more
semanticscholar +1 more source
Journal of Medicinal Chemistry, 2012
(D)-Glucosamine and other nutritional supplements have emerged as safe alternative therapies for osteoarthritis (OA), a chronic and degenerative articular joint disease.
M. Serpi+9 more
semanticscholar +1 more source
(D)-Glucosamine and other nutritional supplements have emerged as safe alternative therapies for osteoarthritis (OA), a chronic and degenerative articular joint disease.
M. Serpi+9 more
semanticscholar +1 more source
Journal of the American Chemical Society, 2012
Numerous biomolecules possess α-D-glucosamine as structural component. However, chemical glycosylations aimed at this backbone are usually not easily attained without generating the unwanted β-isomer.
M. M. Zulueta+14 more
semanticscholar +1 more source
Numerous biomolecules possess α-D-glucosamine as structural component. However, chemical glycosylations aimed at this backbone are usually not easily attained without generating the unwanted β-isomer.
M. M. Zulueta+14 more
semanticscholar +1 more source