Ring-Rearrangement Metathesis of 1-Substituted 7-Azanorbornenes as an Entry to 1-Azaspiro[4.5]decane systems

  1. Carreras, J. 1
  2. Avenoza, A. 1
  3. Busto, J.H. 1
  4. Peregrina, J.M. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Revista:
Journal of Organic Chemistry

ISSN: 0022-3263

Any de publicació: 2011

Volum: 76

Número: 9

Pàgines: 3381-3391

Tipus: Article

DOI: 10.1021/JO200321T SCOPUS: 2-s2.0-79955554628 WoS: WOS:000289956900044 GOOGLE SCHOLAR

Altres publicacions en: Journal of Organic Chemistry

Indicadors

Cites rebudes

  • Cites en Scopus: 19 (08-05-2023)
  • Citas en Web of Science: 17 (20-05-2023)
  • Cites en Dimensions: 18 (30-03-2023)

JCR (Journal Impact Factor)

  • Any 2011
  • Factor d'impacte de la revista: 4.45
  • Factor d'impacte sense autocites: 3.988
  • Article influence score: 1.057
  • Quartil major: Q1
  • Àrea: CHEMISTRY, ORGANIC Quartil: Q1 Posició en l'àrea: 9/56 (Edició: SCIE)

SCImago Journal Rank

  • Any 2011
  • Impacte SJR de la revista: 2.265
  • Quartil major: Q1
  • Àrea: Organic Chemistry Quartil: Q1 Posició en l'àrea: 13/181

Scopus CiteScore

  • Any 2011
  • CiteScore de la revista: 7.7
  • Àrea: Organic Chemistry Percentil: 92
  • Àrea: Medicine (all) Percentil: 89

Dimensions

(Dades actualitzats a data de 30-03-2023)
  • Cites totals: 18
  • Cites recents: 2
  • Relative Citation Ratio (RCR): 0.17
  • Field Citation Ratio (FCR): 2.47

Resum

Several metathesis sequences have been carried out using 7-azanorbornenes as starting materials. The occurrence of several exocyclic olefin patterns in the bridgehead position of this system opens the way to gain interesting spirocyclic compounds, which were achieved using several ring-rearrangement metatheses (RRM). The metathesis products, thus obtained, may be useful for the synthesis of new peptidomimetics and related compounds. © 2011 American Chemical Society.