TfOH-catalyzed regioselective N-alkylation of indazoles with diazo compounds
Chemical Communications, ISSN: 1364-548X, Vol: 58, Issue: 44, Page: 6429-6432
2022
- 17Citations
- 5Captures
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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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Metrics Details
- Citations17
- Citation Indexes17
- 17
- CrossRef11
- Captures5
- Readers5
Article Description
Selective alkylation of indazoles is still a highly challenging topic in chemistry and the synthesis of important molecules. Herein, a novel highly selective N-alkylation of indazoles with diazo compounds is described in the presence of TfOH. Unlike the traditional metal- and base-catalysed version, this protocol highlights the regioselectivity of alkylation of indazoles and a metal-free catalysis system, affording N-alkylated products in good to excellent yields with high regioselectivity (N/N up to 100/0) and excellent functional group tolerance. Furthermore, a gram scale synthesis was conducted successfully to give rise to the corresponding products. Mechanistic studies through control experiments provide plausible mechanistic proposals.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85131226642&origin=inward; http://dx.doi.org/10.1039/d2cc01404a; http://www.ncbi.nlm.nih.gov/pubmed/35546320; https://xlink.rsc.org/?DOI=D2CC01404A; https://dx.doi.org/10.1039/d2cc01404a; https://pubs.rsc.org/en/content/articlelanding/2022/cc/d2cc01404a
Royal Society of Chemistry (RSC)
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