Metal-free oxidative coupling of quinoxalin-2(1: H)-ones with arylaldehydes leading to 3-acylated quinoxalin-2(1 H)-ones
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 16, Issue: 17, Page: 3203-3212
2018
- 130Citations
- 8Captures
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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
- Citations130
- Citation Indexes130
- 130
- CrossRef110
- Captures8
- Readers8
Article Description
A facile TBHP-mediated direct oxidative coupling of quinoxalin-2(1H)-ones with arylaldehydes has been developed under metal-free conditions. This method provided a convenient and efficient approach to various 3-acylated quinoxalin-2(1H)-ones from readily available starting materials with excellent regioselectivity. This reaction proceeded efficiently under mild conditions over a broad range of substrates and with functional group tolerance.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85046655275&origin=inward; http://dx.doi.org/10.1039/c8ob00206a; http://www.ncbi.nlm.nih.gov/pubmed/29658033; https://xlink.rsc.org/?DOI=C8OB00206A; https://dx.doi.org/10.1039/c8ob00206a; https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00206a
Royal Society of Chemistry (RSC)
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