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Journal of Carbohydrate Chemistry is a peer-reviewed journal published by Taylor & Francis, covering Carbohydrate Chemistry and Synthesis, Glycosylation and Glycoproteins Research, Chemical Synthesis and Analysis.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Journal of Carbohydrate Chemistry 12 (3): 45–58.
Formats any DOI in Journal of Carbohydrate Chemistry style. No sign-up. |
| Publishes research in | Carbohydrate Chemistry and Synthesis Glycosylation and Glycoproteins Research Chemical Synthesis and Analysis Enzyme Production and Characterization Microbial Metabolites in Food Biotechnology |
| ISSN | 0732-8303 |
| Citation impact (2-yr) | 1.38 |
| h-index | 58 |
| i10-index | 1,119 |
| Total citations | 32,320 |
| Top institutions publishing here | Centre National de la Recherche Scientifique |
| Journal website | www.tandfonline.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Abstract It is generally acknowledged that information about carbohydrate conformation is important for the understanding of interaction between carbohydrates and other biomolecules, such as proteins.1–5 The major part of oligosaccharides involved in the interactions are made up of hexopyranoses, and the overall conformation can be described by the rotation of the glycosidic linkages and the…
ABSTRACT The primary alcohol groups of ten polysaccharides, with widely different structures and water solubilities, were oxidized to carboxyl groups using 2,2,6,6-tetramethyl-1-piperidine oxoammonium ion (TEMPO) at pH 10.8 and 0°C. The yield and selectivity for the primary alcohol group were high for all ten of the polysaccharides. The oxidation greatly increased the water-solubility of the…
Abstract Regioselective reductive ring openings of 4, 6-O-benzylidene acetals of hexopyranosides are described using borane trimethylamine-aluminium chloride. Using toluene as solvent, 4-O-benzyl ethers with the 6-OH free are obtained. Using tetrahydrofuran as solvent. 6-O-benzyl ethers with the 4-OH free are obtained.
Abstract Recently, great interest has been focussed on the synthesis of oligosaccharides containing N-acetylneuraminic acid (Neu5Ac) because of its important roles in a variety of biological recognitions.2 However, many difficulties in the synthesis of naturally occurring α-glycosides still remained.3 We have recently reported the stereo-selective synthesis of a series of α- and β-2-thio-neuraminyl glycosides.1-4 In…
Abstract The synthesis of a protected pentasaccharide 27b corresponding to the antithrombin III binding region of heparin is presented. This pentasaccharide was prepared from two disaccharides (12c and 23) and a monosaccharide (1). The glucuronic acid containing disaccharide 12c was prepared from easily available monomers 6 and 7. Oxidation to the uronic acid was performed…
