Colacot Thomas J, Shea Helene A
Catalysis & Chiral Technologies, Johnson Matthey, 2001 Nolte Drive, West Deptford, New Jersey 08066, USA.
Org Lett. 2004 Oct 14;6(21):3731-4. doi: 10.1021/ol048598t.
[reaction: see text] The use of Cp(2)Fe(PR(2))(2)PdCl(2) (R = i-Pr and t-Bu) in Suzuki coupling reactions were illustrated using a high throughput screening approach. The di-tbpfPdCl(2) catalyst was shown to be the more active catalyst for unactivated and sterically challenging aryl chlorides. Comparison studies using the commercial catalysts dppfPdCl(2), (Ph(3)P)(2)PdCl(2), (Cy(3)P)(2)PdCl(2), DPEPhosPdCl(2), dppbPdCl(2), dppePdCl(2), Pd(t-Bu(3)P)(2), and Pd(mu-Br)(t-Bu(3)P) were also done for selected cases to demonstrate the superior activities of di-tbpfPdCl(2) and di-isoppfPdCl(2).