Organic Chemistry Portal

Abstracts

Search:

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)


 

Abstract

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



Key Words

aryl ketones, Suzuki Coupling


ID: J42-Y2015