Journal of Carbohydrate Chemistry
Published by Taylor & Francis
ISSN : 0732-8303 eISSN : 1532-2327
Abbreviation : J. Carbohydr. Chem.
Aims & Scope
The Journal of Carbohydrate Chemistry serves as an international forum for research advances involving the chemistry and biology of carbohydrates.
The following aspects are considered to fall within the scope of this journal: -novel synthetic methods involving carbohydrates, oligosaccharides, and glycoconjugates- the use of chemical methods to address aspects of glycobiology- spectroscopic and crystallographic structure studies of carbohydrates- computational and molecular modeling studies- physicochemical studies involving carbohydrates and the chemistry and biochemistry of carbohydrate polymers.
View Aims & ScopeMetrics & Ranking
Impact Factor
Year | Value |
---|---|
2025 | 2.2 |
2024 | 1.20 |
SJR (SCImago Journal Rank)
Year | Value |
---|---|
2024 | 0.369 |
Quartile
Year | Value |
---|---|
2024 | Q3 |
h-index
Year | Value |
---|---|
2024 | 41 |
Journal Rank
Year | Value |
---|---|
2024 | 14619 |
Journal Citation Indicator
Year | Value |
---|---|
2024 | 97 |
Impact Factor Trend
Abstracting & Indexing
Journal is indexed in leading academic databases, ensuring global visibility and accessibility of our peer-reviewed research.
Subjects & Keywords
Journal’s research areas, covering key disciplines and specialized sub-topics in Biochemistry, Genetics and Molecular Biology and Chemistry, designed to support cutting-edge academic discovery.
Most Cited Articles
The Most Cited Articles section features the journal's most impactful research, based on citation counts. These articles have been referenced frequently by other researchers, indicating their significant contribution to their respective fields.
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A Conformational Study of Hydroxymethyl Groups in Carbohydrates Investigated by <sup>1</sup>H NMR Spectroscopy
Citation: 255
Authors: Klaus, Jens Ø
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Reductive Ring Openings of Carbohydrate Benzylidene Acetals Using Borane-Trimethylamine and Aluminium Chloride. Regioselectivity and Solvent Dependance
Citation: 174
Authors: Monica, Per J., Hans, Stefan
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Glycosylation Using Methylthioglycosides of<i>N</i>-Acetylneuraminic Acid and Dimethyl(Methylthio)Sulfonium Triflate
Citation: 166
Authors: Osamu, Makoto, Akira
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Oxidation of Primary Alcohol Groups of Naturally Occurring Polysaccharides with 2,2,6,6-Tetramethyl-1-Piperidine Oxoammonium Ion
Citation: 158
Authors: Pahn S., John F.
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Communication: Synthetic Studies on Sialoglycoconjugates 25: Reactivity of Glycosyl Promoters in α-Glycosylation of N-Acetyl-Neuraminic Acid with the Primary and Secondary Hydroxyl Groups in the Suitably Protected Galactose and Lactose Derivatives
Citation: 154
Authors: Akira, Takao, Hitoshi, Kenji, Hideharu, Makoto
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Synthesis of a Pentasaccharide Corresponding to the Antithrombin III Binding Fragment of Heparin
Citation: 153
Authors: C. A.A., T., J. N., A. J.M., S. F., R. H., J. M. R., F. A.
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<sup>1</sup>H NMR Analyses of Rotameric Distribution of C5-C6 bonds of D-Glucopyranoses in Solution
Citation: 146
Authors: Yoshihiro, Hiroshi, Hiroshi, Hiroshi
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O-(α-D-Glucopyranosyl)trichloroacetimidate as a Glucosyl Donor
Citation: 134
Authors: Richard R., Josef
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Mechanism of Chemical Glycosylation: Focus on the Mode of Activation and Departure of Anomeric Leaving Groups
Citation: 131
Authors: Sneha C., Alexei V.