Synfacts 2008(10): 1085-1085  
DOI: 10.1055/s-2008-1078222
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart ˙ New York

Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl Chlorides

Contributor(s): Paul Knochel, Andrei Gavryushin
S. D. Dreher*, P. G. Dormer, D. L. Sandrock, G. A. Molander*
Merck and Co. Inc., Rahway and University of Pennsylvania, Philadelphia, USA
Further Information

Publication History

Publication Date:
22 September 2008 (online)

Significance

This valuable synthetic method demonstrates the usefulness of the parallel microscale experimentation approach in the development of new methodology in synthetic chemistry. Conditions for a smooth Pd-catalyzed cross-coupling between secondary alkyltrifluoroborates and aryl or heteroaryl chlorides have been found after the screening of a number of phosphine ligands. The parallel microscale experimentation is proved to be a very promising method of investigation in synthetic chemistry that will find more and more applications not only in industry, but also in the academic research.