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

Revue:
Journal of Organic Chemistry

ISSN: 0022-3263

Année de publication: 2011

Volumen: 76

Número: 9

Pages: 3381-3391

Type: Article

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

D'autres publications dans: Journal of Organic Chemistry

Indicateurs

Cité par

  • Scopus Cité par: 19 (06-06-2023)
  • 'Web of Science' Cité par: 17 (20-05-2023)
  • Dimensions Cité par: 18 (30-03-2023)

JCR (Journal Impact Factor)

  • Año 2011
  • Factor de impacto de la revista: 4.45
  • Factor de impacto sin autocitas: 3.988
  • Article influence score: 1.057
  • Cuartil mayor: Q1
  • Área: CHEMISTRY, ORGANIC Cuartil: Q1 Posición en el área: 9/56 (Edicion: SCIE)

SCImago Journal Rank

  • Año 2011
  • Impacto SJR de la revista: 2.265
  • Cuartil mayor: Q1
  • Área: Organic Chemistry Cuartil: Q1 Posición en el área: 13/182

Scopus CiteScore

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

Dimensions

(Datos actualizados a fecha de 30-03-2023)
  • Citas totales: 18
  • Citas recientes: 2
  • Relative Citation Ratio (RCR): 0.17
  • Field Citation Ratio (FCR): 2.47

Résumé

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.