Metal-free arylation of benzene and pyridine promoted by amino-linked nitrogen heterocyclic carbenes
Chemical Communications, ISSN: 1364-548X, Vol: 48, Issue: 53, Page: 6702-6704
2012
- 117Citations
- 71Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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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
- Citations117
- Citation Indexes117
- 117
- CrossRef113
- Captures71
- Readers71
- 71
Article Description
An amino-linked nitrogen heterocyclic carbene (amino-NHC), 1-tBu, has been shown to mediate carbon-carbon coupling through the direct C-H functionalization of benzene and pyridine in the absence of a metal catalyst. Using EPR, the first spectroscopic evidence corroborating the single electron transfer mechanism for the metal-free carbon-carbon coupling manifold, as reported by others, is introduced. © 2012 Royal Society of Chemistry.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84862167141&origin=inward; http://dx.doi.org/10.1039/c2cc32519e; http://www.ncbi.nlm.nih.gov/pubmed/22627744; https://xlink.rsc.org/?DOI=c2cc32519e; https://dx.doi.org/10.1039/c2cc32519e; https://pubs.rsc.org/en/content/articlelanding/2012/cc/c2cc32519e
Royal Society of Chemistry (RSC)
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