Nickel-Catalyzed Direct Cross-Coupling of Aryl Thioether with Aryl Bromide.
Na-Na MaXuan-Bo HuYuan-Shuai WuYa-Wen ZhengMengtao MaXue-Qiang ChuHao XuHaiqing LuoZhi-Liang ShenPublished in: Organic letters (2023)
A straightforward cross-coupling of aryl thioether with aryl bromide with the aid of nickel salt, magnesium, and lithium chloride in tetrahydrofuran at ambient temperature was accomplished. The one-pot reactions proceeded efficiently via C-S bond cleavage to produce the desired biaryls in modest to good yields, avoiding the use of pregenerated or commercial organometallic reagents.