Ligand-enabled palladium-catalyzed hydroesterification of vinyl arenes with high linear selectivity to access 3-arylpropanoate esters
Chemical Communications, ISSN: 1364-548X, Vol: 58, Issue: 24, Page: 3921-3924
2022
- 12Citations
- 4Captures
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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
- Citations12
- Citation Indexes12
- 12
- CrossRef11
- Captures4
- Readers4
Article Description
Palladium-catalyzed linear-selective hydroesterification of vinyl arenes with alcohols enabled by diphosphine ligands derived from bis[2-(diphenylphosphino)ethyl]amides has been developed. A variety of 3-arylpropanoate esters were obtained in high yields and regioselectivity. The robustness of this methodology was further demonstrated by the efficient gram-scale synthesis of the ethyl 3-phenylpropanoate as a precursor to hydrocinnamic acid.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85127090943&origin=inward; http://dx.doi.org/10.1039/d2cc00228k; http://www.ncbi.nlm.nih.gov/pubmed/35244116; https://xlink.rsc.org/?DOI=D2CC00228K; https://dx.doi.org/10.1039/d2cc00228k; https://pubs.rsc.org/en/content/articlelanding/2022/cc/d2cc00228k
Royal Society of Chemistry (RSC)
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