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  • New catalysts for Suzuki-Miyaura coupling reactions of heteroatom-substituted heteroaryl chlorides.

New catalysts for Suzuki-Miyaura coupling reactions of heteroatom-substituted heteroaryl chlorides.

The Journal of organic chemistry (2007-06-07)
Anil S Guram, Xiang Wang, Emilio E Bunel, Margaret M Faul, Robert D Larsen, Michael J Martinelli
ABSTRACT

The new air-stable PdCl2[PR2(Ph-R')]2 complexes, readily prepared from commercial reagents, exhibit unique efficiency as catalysts for the Suzuki-Miyaura coupling reactions of a variety of heteroatom-substituted heteroaryl chlorides with a diverse range of aryl/heteroaryl boronic acids. The coupling reactions catalyzed by the new complexes exhibit high product yields (88-99%) and high catalyst turnover numbers (up to 10,000 TON).

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Bis[di-(tert-butyl)(4-trifluoromethylphenyl)phosphine]palladium(II) chloride
Sigma-Aldrich
Dichlorobis(di-tert-butylphenylphosphine)palladium(II), 95%