Rhodium-catalyzed C-H activation of hydrazines leads to isoquinolones with tunable aggregation-induced emission properties
Chemical Communications, ISSN: 1364-548X, Vol: 51, Issue: 76, Page: 14365-14368
2015
- 51Citations
- 18Captures
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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
- Citations51
- Citation Indexes51
- 51
- CrossRef49
- Captures18
- Readers18
- 18
Article Description
Using an internally oxidizing directing group (DG) strategy, we report a Rh-catalyzed synthesis of isoquinolones via C-H activation/annulation of benzoylhydrazines and alkynes. Tunable double cascade cyclization of benzoylhydrazines with two equivalents of alkynes led to tetracyclic amides. These N-heterocycles demonstrated adjustable AIE properties.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84941203312&origin=inward; http://dx.doi.org/10.1039/c5cc05239d; http://www.ncbi.nlm.nih.gov/pubmed/26268790; http://xlink.rsc.org/?DOI=C5CC05239D; http://pubs.rsc.org/en/content/articlepdf/2015/CC/C5CC05239D; https://xlink.rsc.org/?DOI=C5CC05239D; https://dx.doi.org/10.1039/c5cc05239d; https://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc05239d
Royal Society of Chemistry (RSC)
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