Temporary (P=O) directing group enabled carbazoleorthoarylationviapalladium catalysis
Chemical Communications, ISSN: 1364-548X, Vol: 57, Issue: 16, Page: 2021-2024
2021
- 16Citations
- 10Captures
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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
- Citations16
- Citation Indexes16
- 16
- CrossRef10
- Captures10
- Readers10
Article Description
A palladium-catalyzed, temporary P(O) directing group assisted C-H bond arylation of carbazoles was achieved. The release of the directing group occurs spontaneously in the reaction and the mechanistic studies indicate that acid is essential for N-P bond cleavage.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85101502599&origin=inward; http://dx.doi.org/10.1039/d0cc07596e; http://www.ncbi.nlm.nih.gov/pubmed/33506237; https://xlink.rsc.org/?DOI=D0CC07596E; https://dx.doi.org/10.1039/d0cc07596e; https://pubs.rsc.org/en/content/articlelanding/2021/cc/d0cc07596e
Royal Society of Chemistry (RSC)
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