Binuclear Palladium Complex Immobilized on Mesoporous SBA-16: Efficient Heterogeneous Catalyst for the Carbonylative Suzuki Coupling Reaction of Aryl Iodides and Arylboronic Acids Using Cr(CO)6 as Carbonyl Source

Author:

Niakan Mahsa,Asadi Zahra,Emami Mohammad

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry,Catalysis

Reference67 articles.

1. Gautam P, Tiwari NJ, Bhanage BM (2019) Aminophosphine palladium pincer-catalyzed carbonylative sonogashira and Suzuki-Miyaura cross-coupling with high catalytic turnovers. ACS Omega 4:1560–1574

2. You S, Yan C, Zhang R, Cai M (2019) A convenient and practical heterogeneous palladium-catalyzed carbonylative Suzuki coupling of aryl iodides with formic acid as carbon monoxide source. Appl Organomet Chem 33:e4650

3. Bjerglund KM, Skrydstrup T, Molander GA (2014) Carbonylative Suzuki couplings of aryl bromides with boronic acid derivatives under base-free conditions. Org Lett 16:1888–1891

4. Gautam P, Bhanage BM (2015) Palladacycle catalyzed carbonylative Suzuki-Miyaura coupling with high turnover number and turnover frequency. J Org Chem 80:7810–7815

5. Boubakri L, Al-Ayed AS, Mansour L, Harrath AA, Al-Tamimi J, Özdemir I, Yasar S, Hamdi N (2019) In situ palladium/NH heterocyclic carbene complex catalyzed carbonylative cross-coupling reactions of arylboronic acids with 2-bromopyridine under CO pressure: efficient synthesis of unsymmetrical arylpyridine ketones and their antimicrobial activities. Catal Lett 44:321–328

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