Ene cyclization reaction in heterocycle synthesis
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 16, Issue: 16, Page: 2820-2840
2018
- 28Citations
- 15Captures
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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
- Citations28
- Citation Indexes28
- CrossRef28
- 26
- Captures15
- Readers15
- 15
Review Description
The ene cyclization has evolved to become an indispensable tool for the synthesis of various ring size heterocyclic compounds. In the past and recent years, many exciting reports have demonstrated the broad scope and synthetic utility of ene cyclization and the versatility of oxonium ion, iminium ion and thionium ion intermediates. Moreover, the ease of regio- and stereoselectivity of ene cyclization has led to the development of new types of heterocyclic compounds. This article aims at reviewing the utilities of ene cyclization reactions for the synthesis of various ring sizes of oxygen, nitrogen and sulfur heterocycles. It also covers some applications in natural product synthesis. The mechanism of the reactions is discussed wherever necessary. The review article covers the time period from 1986 to 2017.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85046009152&origin=inward; http://dx.doi.org/10.1039/c8ob00429c; http://www.ncbi.nlm.nih.gov/pubmed/29594296; https://xlink.rsc.org/?DOI=C8OB00429C; https://dx.doi.org/10.1039/c8ob00429c; https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00429c
Royal Society of Chemistry (RSC)
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