Cu-catalyzed suzuki-miyaura reactions of primary and secondary benzyl halides with arylboronates
Chemical Communications, ISSN: 1364-548X, Vol: 50, Issue: 75, Page: 11060-11062
2014
- 84Citations
- 50Captures
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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
- Citations84
- Citation Indexes84
- 84
- CrossRef73
- Captures50
- Readers50
- 50
Article Description
A copper-catalyzed Suzuki-Miyaura coupling of benzyl halides with arylboronates is described. Varieties of primary benzyl halides as well as more challenging secondary benzyl halides with β hydrogens or steric hindrance could be successfully converted into the corresponding products. Thus it provides access to diarylmethanes, diarylethanes and triarylmethanes. © 2014 The Partner Organisations.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84906536106&origin=inward; http://dx.doi.org/10.1039/c4cc05376a; http://www.ncbi.nlm.nih.gov/pubmed/25102380; http://xlink.rsc.org/?DOI=C4CC05376A; http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC05376A; https://xlink.rsc.org/?DOI=C4CC05376A; https://dx.doi.org/10.1039/c4cc05376a; https://pubs.rsc.org/en/content/articlelanding/2014/cc/c4cc05376a
Royal Society of Chemistry (RSC)
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