Table 2.

Substrate Scope of Aryl and Heteroaryl Halides.^a

(A) Aryl halides
11a, 67%, X = Br α/γ = 98:2	11b, 74%, X = Br α/γ = 97:3	11c, 61%, X = Br α/γ = 98:2	11g, 81% (95%), X = Br γ/α > 99:1	11h, 96%, X = Br γ/α > 99:1	11I, 95%, X = Br γ/α > 99:1
11d, (69%), X = Br α/γ > 99:1	11e, 85%, X = Br α/γ > 99:1	11f, 75% (84%), X = Br, α/γ = 98:2 (89%), X = CI, α/γ = 98:2 (96%), X = OTf, α/γ = 98:2	11J, 70% (80%), X = Br γ/α < 99:1	11k, 90%, X = Br γ/α > 99:1	11I, 90%, (95%), X = Br, γ/α > 99:1 (97%), X = CI, γ/α = 99:1 (95%), X = OTf, γ/α > 99:1
(B) Heteroaryl halides
11m, 75%, X = Br α/γ = 99:1	11n, 75%, X = Br α/γ = 99:1	11o, 86%, X=Br α/γ > 99:1b	11s, 97%, X = Br γ/α > 99:1	11t, 85%, X = CI γ/α > 99:1	11u, 62%c, X = CI γ/α > 99:1
11p, 54% (75%), X = Br α/γ > 99:1b	11q, 85%, X = Br α/γ > 99:1b	11r, 97%, X = CI α/γ > 99:1b	11v, 77%, X = CI γ/α > 99:1	11w, 93%, X = Br γ/α > 99:1	11x, 78%, X = CI γ/α > 99:1

^aYields are of isolated product, see Supporting Information for details; α/γ ratio and yields in parentheses were determined by ¹H NMR spectroscopy of the crude reaction mixture using 1,3,5-trimethoxybenzene as an internal standard.

^bL5 was used instead of L6.

^c60 °C.