Solvent- and transition metal-free amide synthesis from phenyl esters and aryl amines
RSC Advances, ISSN: 2046-2069, Vol: 9, Issue: 3, Page: 1536-1540
2019
- 22Citations
- 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
- Citations22
- Citation Indexes22
- 22
- CrossRef20
- Captures18
- Readers18
- 18
Article Description
A general, economical, and environmentally friendly method of amide synthesis from phenyl esters and aryl amines was developed. This new method has significant advantages compared to previously reported palladium-catalyzed approaches. The reaction is performed transition metal- and solvent-free, using a cheap and environmentally benign base, NaH. This approach enabled us to obtain target amides in high yields with high atom economy.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85060179896&origin=inward; http://dx.doi.org/10.1039/c8ra10040c; http://www.ncbi.nlm.nih.gov/pubmed/35518015; https://xlink.rsc.org/?DOI=C8RA10040C; https://dx.doi.org/10.1039/c8ra10040c; https://pubs.rsc.org/en/content/articlelanding/2019/ra/c8ra10040c
Royal Society of Chemistry (RSC)
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