Palladacycle-Catalyzed Carbonylative Suzuki-Miyaura Coupling with High Turnover Number and Turnover Frequency
Prashant Gautam and Bhalchandra M. Bhanage*
*Department of Chemistry, Institute of Chemical Technology, N.P. Marg, Matunga-400019, Mumbai, India, Email: bm.bhanageictmumbai.edu.in
P. Gautam, B. M. Bhanage, J. Org. Chem., 2015, 80, 7810-7815.
DOI: 10.1021/acs.joc.5b01160 (free Supporting Information)
Palladacycles catalyze a carbonylative Suzuki-Miyaura coupling of aryl iodides with arylboronic acids with high turnover numbers and turnover frequencies. Comparison of the palladacycles with a conventional palladium source shows their superiority.
see article for more examples