Mechanism of Benzoquinone-Promoted Palladium-Catalyzed Oxidative Cross-Coupling Reactions

被引:211
作者
Hull, Kami L. [1 ]
Sanford, Melanie S. [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
关键词
C-H BONDS; DIRECT ARYLATION; ACTIVATION; FUNCTIONALIZATION; COMPLEXES; ARENES;
D O I
10.1021/ja901952h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Presented) This communication describes mechanistic studies of the Pd-catalyzed oxidative cross-coupling of benzo[h]quinoline with simple arenes. Through a series of experiments, including determination of the order of the reaction in various reagents, H/D exchange studies, kinetic isotope effect investigations, and the evaluation of electronic effects, we propose a detailed mechanism for these reactions. Importantly, this mechanism explains the key role of benzoquinone in these transformations; in addition, it provides insights that allow the rational tuning of reaction conditions to control the chemoselectivity of Ar-Ar′ coupling. © 2009 American Chemical Society.
引用
收藏
页码:9651 / 9653
页数:3
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