138034-97-6Relevant academic research and scientific papers
Preparation of Vinyl Arenes by Nickel-Catalyzed Reductive Coupling of Aryl Halides with Vinyl Bromides
Liu, Jiandong,Ren, Qinghua,Zhang, Xinghua,Gong, Hegui
supporting information, p. 15544 - 15548 (2016/12/09)
This work emphasizes the synthesis of substituted vinyl arenes by reductive coupling of aryl halides with vinyl bromides under mild and easy-to-operate nickel-catalyzed reaction conditions. A broad range of aryl halides, including heteroaromatics, and vinyl bromides were employed to yielding products in moderate to excellent yields with high functional-group tolerance. The nickel-catalytic system displays good chemoselectivity between the two C(sp2)-halide coupling partners, thus demonstrating a mechanistic pathway distinct from other stepwise protocols.
Vinyl Cation Formation by Decomposition of Vinyllead(IV) Triacetates. Part 2.
Pinhey, John T.,Stoermer, Martin J.
, p. 2455 - 2460 (2007/10/02)
The products resulting from the reductive elimination of lead(II) acetate from four E- and Z-pairs of vinyllead triacetates have been examined for evidence that these highly unstable lead compounds are a potential source of vinyl cations, including the le
