Article detail · 2013
Palladium Catalyzed Mizoroki-Heck and Suzuki-Miyaura Reactions Using Napthalenomethyl-Substituted Imidazolidin-2-ylidene Ligands in Aqueous Media
- Year
- 2013
- Type
- article
Data source split
- YÖKSİS YÖKSİS article record
- YÖKSİS venue JOURNAL OF COORDINATION CHEMISTRY
- Catalog match (ISSN) Journal of Coordination Chemistry
- OpenAlex OpenAlex enrichment (abstract, citations, topics)
Abstract
OpenAlex · English
Naphthalenomethyl-substituted imidazolidinium salts (1a-g) were prepared and characterized by conventional spectroscopic methods, 1H NMR, 13C NMR, FTIR, and elemental analysis techniques. The in situ prepared three component systems naphthalenomethyl-substituted imidazolidinium salts, Pd(OAc)2, and K2CO3 catalyzed quantitatively the Mizoroki–Heck and Suzuki–Miyaura coupling of aryl halides under mild conditions in aqueous media.
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Citations
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37 citations
OpenAlex cited_by_count (cache / database)
37 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
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