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Spectroscopic Studies of the Chan–Lam Amination: A Mechanism-Inspired Solution to Boronic Ester Reactivity
Journal of the American Chemical Society ( IF 15.0 ) Pub Date : 2017-03-24 , DOI: 10.1021/jacs.6b12800
Julien C. Vantourout 1, 2 , Haralampos N. Miras 3 , Albert Isidro-Llobet 2 , Stephen Sproules 3 , Allan J. B. Watson 1
Affiliation  

We report an investigation of the Chan-Lam amination reaction. A combination of spectroscopy, computational modeling, and crystallography has identified the structures of key intermediates and allowed a complete mechanistic description to be presented, including off-cycle inhibitory processes, the source of amine and organoboron reactivity issues, and the origin of competing oxidation/protodeboronation side reactions. Identification of key mechanistic events has allowed the development of a simple solution to these issues: manipulating Cu(I) → Cu(II) oxidation and exploiting three synergistic roles of boric acid has allowed the development of a general catalytic Chan-Lam amination, overcoming long-standing and unsolved amine and organoboron limitations of this valuable transformation.

中文翻译:

Chan-Lam 胺化的光谱研究:一种受机制启发的硼酸酯反应性解决方案

我们报告了对 Chan-Lam 胺化反应的调查。光谱学、计算模型和晶体学的结合已经确定了关键中间体的结构,并允许呈现完整的机制描述,包括非循环抑制过程、胺和有机硼反应性问题的来源,以及竞争氧化的起源/原脱硼副反应。关键机制事件的识别使得开发出解决这些问题的简单方法:操纵 Cu(I) → Cu(II) 氧化和利用硼酸的三种协同作用,开发了通用催化 Chan-Lam 胺化,克服了这种有价值的转化长期存在且未解决的胺和有机硼限制。
更新日期:2017-03-24
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