An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers

Angew Chem Int Ed Engl. 1998 Sep 18;37(17):2387-2390. doi: 10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M.

Abstract

Since the pioneering work of Wurtz, cross-couplings between sp3 carbon centers have had the reputation of being difficult. In the presence of a catalytic amount of m-trifluoromethylstyrene, an efficient cross-coupling reaction takes place between polyfunctional primary alkyl iodides and diorganozinc compounds [Eq. (a)] to give a general catalytic cross-coupling between sp3 carbon centers. Piv=pivaloyl; Pent = pentyl; acac = acetalacetonate; NMP = N-methylpyrrolidone.

Keywords: Cross-coupling; Homogeneous catalysis; Nickel; Styrene; Zinc.