Cationic cyclization reactions with alkyne terminating groups: a useful tool in biomimetic synthesis
Chemical Communications, ISSN: 1364-548X, Vol: 58, Issue: 8, Page: 1089-1099
2022
- 10Citations
- 2Captures
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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.
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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
- Citations10
- Citation Indexes10
- 10
- CrossRef8
- Captures2
- Readers2
Article Description
Cyclization reactions through cationic intermediates have become a highly valuable tool in organic synthesis. The use of alkynes as the terminating group in this type of cationic process offers wide synthetic possibilities because this group can serve as a precursor of different functionalities. This article shows relevant examples of cationic cyclization reactions with alkynes as terminating groups with the intention of demonstrating the potential of this type of process, particularly in the context of biomimetic synthesis of natural products.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85123767619&origin=inward; http://dx.doi.org/10.1039/d1cc05826f; http://www.ncbi.nlm.nih.gov/pubmed/34989726; https://xlink.rsc.org/?DOI=D1CC05826F; https://dx.doi.org/10.1039/d1cc05826f; https://pubs.rsc.org/en/content/articlelanding/2022/cc/d1cc05826f
Royal Society of Chemistry (RSC)
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