Ring-Rearrangement Metathesis of 1-Substituted 7-Azanorbornenes as an Entry to 1-Azaspiro[4.5]decane systems
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Universidad de La Rioja
info
ISSN: 0022-3263
Year of publication: 2011
Volume: 76
Issue: 9
Pages: 3381-3391
Type: Article
More publications in: Journal of Organic Chemistry
Metrics
Cited by
JCR (Journal Impact Factor)
- Year 2011
- Journal Impact Factor: 4.45
- Journal Impact Factor without self cites: 3.988
- Article influence score: 1.057
- Best Quartile: Q1
- Area: CHEMISTRY, ORGANIC Quartile: Q1 Rank in area: 9/56 (Ranking edition: SCIE)
SCImago Journal Rank
- Year 2011
- SJR Journal Impact: 2.265
- Best Quartile: Q1
- Area: Organic Chemistry Quartile: Q1 Rank in area: 13/181
Scopus CiteScore
- Year 2011
- CiteScore of the Journal : 7.7
- Area: Organic Chemistry Percentile: 92
- Area: Medicine (all) Percentile: 89
Dimensions
(Data updated as of 30-03-2023)- Total citations: 18
- Recent citations: 2
- Relative Citation Ratio (RCR): 0.17
- Field Citation Ratio (FCR): 2.47
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Abstract
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.