A5113532590- Carbohydrate Chemistry and Synthesis
- Glycosylation and Glycoproteins Research
- Hybrid Renewable Energy Systems
- Marine Sponges and Natural Products
- Hydrogen Storage and Materials
- Fuel Cells and Related Materials
- Oxidative Organic Chemistry Reactions
- Chemical Synthesis and Analysis
- Amino Acid Enzymes and Metabolism
- Traditional and Medicinal Uses of Annonaceae
- Advanced battery technologies research
- Chemical Synthesis and Reactions
- Synthetic Organic Chemistry Methods
- Enzyme Production and Characterization
- Synthesis and Reactivity of Heterocycles
- TiO2 Photocatalysis and Solar Cells
- Monoclonal and Polyclonal Antibodies Research
- Lysosomal Storage Disorders Research
- Cancer therapeutics and mechanisms
- Enzyme Catalysis and Immobilization
- Vanadium and Halogenation Chemistry
- Catalysis and Hydrodesulfurization Studies
- Cyclopropane Reaction Mechanisms
- Microbial Natural Products and Biosynthesis
- Electrocatalysts for Energy Conversion
Harbin Institute of Technology
2024
University of Notre Dame
2004-2019
Nanjing University
2015-2017
Shanghai Genon Biological Products (China)
2014
China Railway Construction Corporation (China)
2014
Chinese Academy of Sciences
2000-2006
Shanghai Institute of Organic Chemistry
2000-2004
Stockholm University
2004
Ottawa University
2000
University of Ottawa
1995-1999
Methyl α- and β-pyranosides of d-glucose d-galactose 1−4 were prepared containing single sites 13C-enrichment at C4, C5, C6 (12 compounds), 1H 13C{1H} NMR spectra obtained to determine a complete set J-couplings (1J, 2J, 3J) involving the labeled carbon nearby protons carbons within exocyclic hydroxymethyl group (CH2OH) each compound. In parallel theoretical studies, dependencies 1J, 3J 13C on C5−C6 (ω) C6−O6 (θ) torsion angles in aldohexopyranoside model compounds computed using density...
ABSTRACT An efficient methodology for regiospecific glycosylation was developed by using 6-O-tert-butyldiphenylsilyl N-acetylglucosamine derivatives 3 and 5 which bear two free hydroxyl groups as acceptors. The regiospecificity attributed to the presence of tert-butyldiphenylsilyl group at O-6 position derivatives. Glycosylation suitably protected galactoside donors 10-14 with acceptors gave only β (1→4) linked disaccharides 15-19 in good yields. Fucosylation disaccharide 18 led Lewis X...
Abstract A facile method for deblocking of dithianes is described. Diacetoxyiodobenzene was used as a cheaper variant bis(trifluoroacetoxy)iodobenzene the regeneration carbonyl compounds from dithianes.
Reaction of a galactosylated 2-C-(hydroxymethyl)-tetrofuranose with paramolybdate ion-exchange resin in aqueous solution at 67 degrees C gave an equililibrium mixture containing the reactant aldofuranose (42%) and 2-ketopentofuranose O1 (58%). Observation this stereospecific rearrangement supports prior arguments that substituents C2 branched-chain are located sterically accessible pocket putative dimolybdate-saccharide reactive complex during epimerization. This provides new convenient...
In this paper, the suitable molecular weight of polyethylene glycol (PEG) and annealing temperature for dye-sensitized solar cells (DSSCs) anode was obtained by assessing performance DSSCs. The output current characteristic DSSCs is to explore factors that affect cell conversion efficiency effect mechanism. Experimental results show 500°C adding PEG 2000, TiO2 thin film electrode has good optical properties.
The crystal structure of methyl α-D-mannopyranosyl-(1→3)-2- O -acetyl-β-D-mannopyranoside monohydrate, C 15 H 26 12 ·H 2 O, ( II ), has been determined and the structural parameters for its constituent α-D-mannopyranosyl residue compared with those α-D-mannopyranoside. Mono- -acetylation appears to promote crystallization inferred from difficulty in crystallizing α-D-mannopyranosyl-(1→3)-β-D-mannopyranoside despite repeated attempts. conformational properties -acetyl side chain ) are similar...
Abstract The strategy to synthesize target compounds (I) and (II) via the key intermediates ethyl 8‐acetylindolizine‐5‐carboxylate methyl 5‐formylindolizine‐8‐carboxylate, resp., is outlined.
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access Abstract, please click on HTML or PDF.
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”