第15章。过渡金属催化的末端炔烃在水中的亲核加成:发展及合成应用

Zoë Hearne, S. Keys, Chao‐Jun Li
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摘要

本章总结了有关在不同范围的不饱和亲电试剂上加成末端炔以制备烷基化分子的亲核文献。与传统方法不同的是,通过使用化学计量量的高活性金属乙酰酯来实现这种转化,因此需要惰性和无水的条件,本文描述的过渡金属催化反应可以在水中进行,这是一种良性且容易获得的溶剂。除了概述一步加成末端炔到亲电试剂的转化外,还讨论了多组分和串联反应。此外,为了提供一个更完整的资源,化学家寻求更可持续的路线合成目标,简要介绍了烷基化反应产物的合成用途。
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CHAPTER 15. Transition Metal-catalysed Nucleophilic Additions of Terminal Alkynes in Water: Development and Synthetic Utility
This chapter summarises the literature concerning the nucleophilic addition of terminal alkynes to a varied scope of unsaturated electrophiles to prepare alkynylated molecules. Unlike classical methods that achieve this transformation by employing stoichiometric quantities of highly reactive metal acetylides and therefore require inert and anhydrous conditions, the transition metal-catalysed reactions described herein can be conducted in water, a benign and readily available solvent. In addition to overviewing transformations for the one-step addition of terminal alkynes to electrophiles, multi-component and tandem reactions are addressed. Furthermore, to offer a more complete resource for chemists seeking more sustainable routes to synthetic targets, a brief survey of the synthetic utility of the alkynylated reaction products is provided.
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