Access to distal meta-C-H functionalization of arylmethanesulfonic acid derivatives
Chemical Communications, ISSN: 1364-548X, Vol: 59, Issue: 59, Page: 9106-9109
2023
- 4Citations
- 1Captures
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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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Article Description
Herein, we report the meta-C-H olefination of arylmethanesulfonates aided by a potentially versatile aliphatic nitrile-directing group under microwave irradiation conditions with fair to very good yields and good to outstanding regioselectivities. Significantly, the protocol showed broad substrate scope including olefin-derived drugs and cyclic olefins. Remarkably, a dual meta-C-H bond was amenable to generating the bis-olefination products.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85165285693&origin=inward; http://dx.doi.org/10.1039/d3cc02260a; http://www.ncbi.nlm.nih.gov/pubmed/37403674; https://xlink.rsc.org/?DOI=D3CC02260A; https://dx.doi.org/10.1039/d3cc02260a; https://pubs.rsc.org/en/content/articlelanding/2023/cc/d3cc02260a
Royal Society of Chemistry (RSC)
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