化学
芳基
催化作用
镍
基质(水族馆)
氘
选择性
偶联反应
还原消去
有机化学
组合化学
量子力学
海洋学
物理
地质学
烷基
作者
Eleanor R. Barber,Hannah M. Hynds,Claudia P. Stephens,Holli E. Lemons,Emily T. Fredrickson,Dale J. Wilger
标识
DOI:10.1021/acs.joc.9b01556
摘要
An operationally simple nickel-catalyzed hydroarylation reaction for alkynes is described. This three-component coupling reaction utilizes commercially available alkynes and aryl bromides, along with water and Zn. An air-stable and easily synthesized Ni(II) precatalyst is the only entity used in the reaction that is not commercially available. This reductive cross-coupling reaction displays a fairly unusual anti selectivity when aryl bromides with ortho substituents are used. In addition to optimization data and a preliminary substrate scope, complementary experiments including deuterium labeling studies are used to provide a tentative catalytic mechanism. We believe this report should inspire and inform other Ni-catalyzed carbofunctionalization reactions.
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