Synthesis and conformational analysis of neoglycoconjugates derived from O- and S-glucose

  1. Rojas, V. 1
  2. Carreras, J. 1
  3. Corzana, F. 1
  4. Avenoza, A. 1
  5. Busto, J.H. 1
  6. Peregrina, J.M. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Journal:
Carbohydrate Research

ISSN: 0008-6215

Year of publication: 2013

Volume: 373

Pages: 1-8

Type: Article

DOI: 10.1016/J.CARRES.2013.02.013 PMID: 23545325 SCOPUS: 2-s2.0-84875403673 WoS: WOS:000319040400001 GOOGLE SCHOLAR

More publications in: Carbohydrate Research

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Metrics

Cited by

  • Scopus Cited by: 4 (12-01-2023)
  • Web of Science Cited by: 4 (31-12-2022)

JCR (Journal Impact Factor)

  • Year 2013
  • Journal Impact Factor: 1.966
  • Journal Impact Factor without self cites: 1.771
  • Article influence score: 0.491
  • Best Quartile: Q2
  • Area: CHEMISTRY, APPLIED Quartile: Q2 Rank in area: 22/71 (Ranking edition: SCIE)
  • Area: BIOCHEMISTRY & MOLECULAR BIOLOGY Quartile: Q3 Rank in area: 212/291 (Ranking edition: SCIE)
  • Area: CHEMISTRY, ORGANIC Quartile: Q3 Rank in area: 31/58 (Ranking edition: SCIE)

SCImago Journal Rank

  • Year 2013
  • SJR Journal Impact: 0.64
  • Best Quartile: Q2
  • Area: Analytical Chemistry Quartile: Q2 Rank in area: 45/107
  • Area: Organic Chemistry Quartile: Q2 Rank in area: 85/186
  • Area: Medicine (miscellaneous) Quartile: Q2 Rank in area: 1025/3001
  • Area: Biochemistry Quartile: Q3 Rank in area: 233/420

Scopus CiteScore

  • Year 2013
  • CiteScore of the Journal : 4.1
  • Area: Analytical Chemistry Percentile: 67
  • Area: Organic Chemistry Percentile: 66
  • Area: Biochemistry Percentile: 54

Related Projects

Diseño racional de glicopéptidos con aplicaciones en Química Biológica

2013/00007/001

Abstract

Using olefin metathesis as a key step, four neoglycoconjugates incorporating α-. O-glucose, α-. S-glucose or β-. S-glucose as a carbohydrate unit and l-serine or l-cysteine as an amino acid moiety have been synthesized. The four-atom carbon spacer allows the carbohydrate to explore a wide-ranging conformational space, which may have important implications for the molecular recognition of these molecules. © 2013 Elsevier Ltd.