An intramolecular C(sp)-H imination using PhI-m CPBA
Chemical Communications, ISSN: 1364-548X, Vol: 55, Issue: 14, Page: 2066-2069
2019
- 23Citations
- 17Captures
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.
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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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
- Citations23
- Citation Indexes23
- 23
- CrossRef22
- Captures17
- Readers17
- 17
Article Description
Herein, a highly exothermic primary amine-polyvalent iodine reaction has been used successfully for selective functionalization of acidic C(sp)-H groups for a dehydrogenative C-H imination reaction by 4H elimination. Overall, C(sp)-H imination at 1,5 distances was readily done via organocatalysis using PhI (10 mol%)-mCPBA under ambient conditions.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85061391149&origin=inward; http://dx.doi.org/10.1039/c8cc09100e; http://www.ncbi.nlm.nih.gov/pubmed/30688962; https://xlink.rsc.org/?DOI=C8CC09100E; https://dx.doi.org/10.1039/c8cc09100e; https://pubs.rsc.org/en/content/articlelanding/2019/cc/c8cc09100e
Royal Society of Chemistry (RSC)
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