Ni(ii)-catalyzed mono-selective: Ortho -arylation of unactivated aryl C-H bonds utilizing amino acids as a directing group
RSC Advances, ISSN: 2046-2069, Vol: 9, Issue: 19, Page: 10820-10824
2019
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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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Article Description
The nickel(ii)-catalyzed ortho-arylation of unactivated C-H bonds utilizing amino acids as directing groups with aryl iodides or bromides as coupling electrophiles is described. This protocol features excellent mono-selectivity, good regioselectivity, and wide functional group tolerance. Additionally, the obtained products bearing a biaryl motif and an amino acid represent bioactive molecules with wide bioactivities.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85064191572&origin=inward; http://dx.doi.org/10.1039/c9ra00749k; http://www.ncbi.nlm.nih.gov/pubmed/35515296; https://xlink.rsc.org/?DOI=C9RA00749K; https://dx.doi.org/10.1039/c9ra00749k; https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra00749k
Royal Society of Chemistry (RSC)
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