Default: Carbohydrate Research

ISSN: 0008-6215

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Carbohydrate Research Q3 Unclaimed

Elsevier BV United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Carbohydrate Research is a journal indexed in SJR in Medicine (miscellaneous) and Biochemistry with an H index of 132. It has an SJR impact factor of 0,465 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,465.

Carbohydrate Research focuses its scope in these topics and keywords: acid, synthesis, polysaccharide, polysaccharides, amino, glycosides, nmr, lactobacillus, analogues, reactivity, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

Carbohydrate Research

0,465

SJR Impact factor

132

H Index

202

Total Docs (Last Year)

519

Total Docs (3 years)

8836

Total Refs

1066

Total Cites (3 years)

519

Citable Docs (3 years)

1,98

Cites/Doc (2 years)

43,74

Ref/Doc

Aims and Scope


acid, synthesis, polysaccharide, polysaccharides, amino, glycosides, nmr, lactobacillus, analogues, reactivity, methyl, sugars, oligosaccharides, mannose, abstract, aqueous, calcium, carbohydrate, characterisation, trisaccharide, conformational, derivatives, activity, sp, structural,



Best articles by citations

Characterisation of acidic heteroglycans from Tremella fuciformis Berk with cytokine stimulating activity

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Synthesis of methyl 6-O-beta-inulotriosyl-a-d-glucopyranoside by intermolecular transglycosylation reaction of cycloinulo-oligosaccharide fructanotransferase

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Lipo-oligosaccharide of Campylobacter lari strain PC 637. Structure of the liberated oligosaccharide and an associated extracellular polysaccharide

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Modeling of deoxy- and dideoxyaldohexopyranosyl ring puckering with MM3(92)

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Trisaccharide synthesis by glycosyl transfer from p-nitrophenyl beta-d-N-acetylgalactosaminide on to disaccharide acceptors catalysed by the beta-N-acetylhexosaminidase from Aspergillus oryzae

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Formation of 4-deoxy-glycero-hexo-2,3-diulo-furanose from microthecin

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Synthesis of uridine-5-propylamine derivatives and their use in affinity chromatography of N-acetylglucosaminyltransferases I and II

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C-2 and C-3 oxidation of d-Glc, and C-2 oxidation of d-Gal by pyranose dehydrogenase from Agaricus bisporus

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Selective formation of C-2 azidodeoxy-d-glucose derivatives from d-glucal precursors using the azidonitration reaction

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Synthesis of deoxyfluoro sugars from carbohydrate precursors

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Molecular dynamics study of polygalacturonic acid chains in aqueous solution

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Trialkylsilyl derivatives of cyclomaltoheptaose, cellulose, and amylose: rearrangement during methylation analysis

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SHOW MORE ARTICLES

Formation of amino acids by reaction of glucose and xylose with primary amines

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Transition-metal saccharide chemistry: synthesis and characterization of d-glucose, d-fructose, d-galactose, d-xylose, d-ribose, and maltose complexes of Co(II)

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Synthesis of pyrido[2,3-d]pyrimidine (5-deazapteridine) C-nucleosides from a glycosyl enaminone

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Chemical modification of some methyl (3,4-di-O-acetyl-2-deoxy-2-hydroxyimino-a-d-arabino-hexopyranosid)uronates

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Unusual lactam formation occurring in the synthesis of a biotinylated T-antigen - serine derivative

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Conformational analysis of asperlin by NMR spectroscopy and molecular modeling

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Methods for the assay of 1,5-anhydro-d-fructose and a-1,4-glucan lyase

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A novel synthetic method for a-d-galactofuranose 1,2,5-orthopivalate

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Polymerized cyclomaltoheptaose (beta-cyclodextrin, beta-CDn) inclusion complex formation with chlorogenic acid: solvent effects on thermochemistry and enthalpy-entropy compensation

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The chemical structure of amylose and amylopectin fractions of starch from tobacco leaves during development and diurnally-nocturnally

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Systematic synthesis of sulfated sialyl-a-(2=>3)-neolactotetraose derivatives and their acceptor specificity for an a-(1=>3)-fucosyltransferase (Fuc-TVII) involved in the biosynthesis of L-selectin ligand

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One-step glycosylation and selective deprotection of peracetylated monosaccharides for facile syntheses of allyl glycosides with a free C-2 hydroxyl group

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