Journal
APPLIED ORGANOMETALLIC CHEMISTRY
Volume 26, Issue 7, Pages 342-346Publisher
WILEY-BLACKWELL
DOI: 10.1002/aoc.2869
Keywords
Suzuki-Miyaura coupling; palladium; tetraphosphine
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An easily prepared tetraphosphine N,N,N',N'-tetra(diphenylphosphinomethyl)-1,2-ethylenediamine (1) combined with PdCl2 affords an efficient catalytic system for Suzuki cross-coupling of aryl and heteroaryl bromides. A high turnover number of 750 000 is obtained with the catalyst loading as low as 1?ppm. This catalyst system exhibits good stability and longevity. In this study, a broad scope of substrates is investigated and satisfactory yields are obtained. Copyright (c) 2012 John Wiley & Sons, Ltd.
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