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Synfacts 2008(10): 1085-1085
DOI: 10.1055/s-2008-1078222
DOI: 10.1055/s-2008-1078222
Metal-Mediated Synthesis
© Georg Thieme Verlag
Stuttgart ˙ New YorkCross-Coupling of Secondary Alkyltrifluoroborates with Aryl Chlorides
S. D. Dreher*, P. G. Dormer, D. L. Sandrock, G. A. Molander*
Merck and Co. Inc., Rahway and University of Pennsylvania, Philadelphia, USA
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
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.