Ring-Rearrangement Metathesis of 1-Substituted 7-Azanorbornenes as an Entry to 1-Azaspiro[4.5]decane systems
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1
Universidad de La Rioja
info
ISSN: 0022-3263
Any de publicació: 2011
Volum: 76
Número: 9
Pàgines: 3381-3391
Tipus: Article
Altres publicacions en: Journal of Organic Chemistry
Indicadors
Cites rebudes
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
Projectes relacionats
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.