Intermediates and Mechanism in Iron-Catalyzed Cross-Coupling

被引:81
作者
Sears, Jeffrey D. [1 ]
Neate, Peter G. N. [1 ]
Neidig, Michael L. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
基金
美国国家卫生研究院;
关键词
ARYL GRIGNARD-REAGENTS; SECONDARY ALKYL-HALIDES; CARBENE CATALYSTS; ALKENYL HALIDES; FERRIC SALTS; REACTIVITY; KUMADA; COMPLEXES; PHOSPHINE; BENZYL;
D O I
10.1021/jacs.8b06893
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Iron-catalyzed cross-coupling reactions have attracted significant research interest, as they offer numerous favorable features compared with cross coupling reactions with precious metal catalysis. While this research has contributed to an empirical understanding of iron-catalyzed cross-coupling, the underlying fundamental mechanisms of reaction and structures of catalytically active species have remained poorly defined. The lack of such detail can be attributed to the difficulties associated with studying such iron-catalyzed reactions, where unstable paramagnetic intermediates abound. Recently, the combined application of physical-inorganic spectroscopic methods, concomitant organic product analysis, and air- and temperature-sensitive inorganic synthesis has yielded the most detailed insight currently available on reactivity and mechanism in iron-catalyzed cross-coupling. This Perspective highlights this approach and the limitations of the contributing techniques as well as some of the key features of the catalytic reactions studied and lessons learned.
引用
收藏
页码:11872 / 11883
页数:12
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