Rapidly Activating Pd-Precatalyst for Suzuki-Miyaura and Buchwald-Hartwig Couplings of Aryl Esters
Amira H. Dardir, Patrick R. Melvin, Ryan. M. Davis, Nilay Hazari* and Megan Mohadjer Beromi
*The Department of Chemistry, Yale University, P.O. Box
208107, New Haven, Connecticut 06520, United States, Email: nilay.hazari
yale.edu
A. H. Dardir, P. R. Melvin, R. M. Davis, N. Hazari, M. M. Beromi, J. Org. Chem., 2018, 83, 469-477.
DOI: 10.1021/acs.joc.7b02588
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Abstract
A recently discovered precatalyst enables Pd-catalyzed Suzuki-Miyaura and Buchwald-Hartwig reactions involving cleavage of a C(acyl)-O bond of aryl esters as electrophiles under mild conditions. The Pd(II) precatalyst is highly active due to its fast reduction to a Pd(0) active species.
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Key Words
Buchwald-Hartwig Coupling, Amides
ID: J42-Y2018
