Weak, bidentate chelating group assisted cross-coupling of C(sp)-H bonds in aliphatic acid derivatives with aryltrifluoroborates
Chemical Communications, ISSN: 1364-548X, Vol: 54, Issue: 90, Page: 12766-12769
2018
- 4Citations
- 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
- Citations4
- Citation Indexes4
- CrossRef4
- Captures10
- Readers10
- 10
Article Description
A protocol of Pd(ii)-catalyzed, weak bidentate directing group assisted β-C(sp)-H activation/cross-coupling with organoboron reagents has been achieved, affording arylation of aliphatic acid derivatives that contain α-hydrogen atoms in moderate to good yields. The potential of this method for an asymmetric β-C(sp)-H arylation via desymmetrization was also presented.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85056319514&origin=inward; http://dx.doi.org/10.1039/c8cc07481j; http://www.ncbi.nlm.nih.gov/pubmed/30371701; https://xlink.rsc.org/?DOI=C8CC07481J; https://dx.doi.org/10.1039/c8cc07481j; https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc07481j
Royal Society of Chemistry (RSC)
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