posted on 2004-09-27, 00:00authored byHrant P. Hratchian, Sanjoy K. Chowdhury, Víctor M. Gutiérrez-García, Kande K. D. Amarasinghe, Mary Jane Heeg, H. Bernhard Schlegel, John Montgomery
The mechanism of nickel-catalyzed couplings of an enone, alkyne, and organozinc has
been studied. Adducts of the substrates with nickel(0) have been isolated and characterized,
and their reactivity was examined. A potential intermediate was demonstrated to not be
kinetically competent in catalytic cyclizations. A computational approach employing the
B3LYP density functional method and the 6-31G(d) basis set was used to examine
mechanistic possibilities that were consistent with experimental observations, and a modified
mechanism for the catalytic cyclizations was formulated. The newly proposed mechanism
involves production of an active catalyst that involves a novel interaction between Ni(0)
and dimethylzinc.