Cooperative iodine and photoredox catalysis for direct oxidative lactonization of carboxylic acids
Chemical Communications, ISSN: 1364-548X, Vol: 55, Issue: 7, Page: 933-936
2019
- 39Citations
- 26Captures
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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
- Citations39
- Citation Indexes39
- 39
- CrossRef32
- Captures26
- Readers26
- 26
Article Description
A new method for the formation of γ- and δ-lactones from carboxylic acids through direct conversion of benzylic C-H to C-O bonds is described. The reaction is conveniently induced by visible light and relies on a mild cooperative catalysis by the combination of molecular iodine and an organic dye.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85060078618&origin=inward; http://dx.doi.org/10.1039/c8cc08594c; http://www.ncbi.nlm.nih.gov/pubmed/30601481; https://xlink.rsc.org/?DOI=C8CC08594C; https://dx.doi.org/10.1039/c8cc08594c; https://pubs.rsc.org/en/content/articlelanding/2019/cc/c8cc08594c
Royal Society of Chemistry (RSC)
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