A rhodium-catalyzed transannulation of N -(per)fluoroalkyl-1,2,3-triazoles under microwave conditions-a general route to N -(per)fluoroalkyl-substituted five-membered heterocycles
Chemical Communications, ISSN: 1364-548X, Vol: 54, Issue: 26, Page: 3258-3261
2018
- 53Citations
- 38Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations53
- Citation Indexes53
- 53
- CrossRef51
- Captures38
- Readers38
- 38
Article Description
A rhodium-catalyzed transannulation via ring-opening of N-(per)fluoroalkyl-substituted 1,2,3-triazoles followed by cycloaddition with different nitriles, enol ethers, isocyanates and silyl ketene acetals under microwave heating provided a highly efficient route to previously unreported N-(per)fluoroalkyl-substituted imidazoles, pyrroles, imidazolones and pyrrolones, respectively. These reactions were found to be applicable to the synthesis of a variety of 5-membered heterocycles bearing different (per)fluoroalkyl substituents as well as both electron-donating and electron-withdrawing groups attached to the heterocyclic core.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85044670257&origin=inward; http://dx.doi.org/10.1039/c8cc01446a; http://www.ncbi.nlm.nih.gov/pubmed/29537032; https://xlink.rsc.org/?DOI=C8CC01446A; https://dx.doi.org/10.1039/c8cc01446a; https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc01446a
Royal Society of Chemistry (RSC)
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