Catalytic transformations of alkenes via nickelacycles

Meng-Ying Qian , Kai-Xiang Zhang , Li-Jun Xiao
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Abstract

Alkenes are fundamental components in synthetic chemistry, extensively used in the production of complex molecules for pharmaceuticals, materials science, and agrochemicals. Nickel-catalyzed transformations of alkenes via nickelacycle intermediates, formed by the oxidative cyclization of alkenes with other π-components on Ni(0), offer a promising approach characterized by high atom and step economy. Although numerous C–C bond formation reactions involving nickelacycles have been widely studied, there is a notable scarcity of comprehensive reviews that focus on transformations of alkenes. Recent progress in ligand design has enhanced control over reactivity and selectivity, enabling a variety of nickel-catalyzed couplings. These include reactions of alkenes with carbon dioxide, isocyanates, alkynes, α,β-unsaturated carbonyls, aldehydes, ketones, and imines. This lack of in-depth discussion highlights the need for a detailed review that encompasses recent advancements in this field. This review summarizes these recent developments in nickel-catalyzed transformations of alkenes via nickelacycles, highlighting the advantages and challenges of this innovative strategy. The goal is to inspire new researchers to explore and contribute to this dynamic field, emphasizing nickelacycle intermediates as versatile tools for effective reactions with various π-components and identifying them as promising avenues for future research.

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通过镍环催化烯烃转化
烯是合成化学中的基本成分,广泛用于生产医药、材料科学和农用化学品中的复杂分子。烯与其他 π 成分在 Ni(0) 上氧化环化形成的镍环中间体,通过镍催化烯的转化提供了一种前景广阔的方法,其特点是原子和阶跃经济性高。尽管涉及镍环的众多 C-C 键形成反应已得到广泛研究,但以烯的转化为重点的全面综述却明显不足。配体设计方面的最新进展提高了控制反应性和选择性,使各种镍催化偶联反应成为可能。这些反应包括烯与二氧化碳、异氰酸酯、炔、α,β-不饱和羰基、醛、酮和亚胺的反应。由于缺乏深入的讨论,因此有必要对这一领域的最新进展进行详细综述。本综述总结了镍催化烯烃通过镍环转化的最新进展,强调了这一创新策略的优势和挑战。目的是激励新的研究人员探索这一充满活力的领域并做出贡献,同时强调镍环中间体是与各种 π 成分进行有效反应的多功能工具,并将其确定为未来研究的前景广阔的途径。
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7.80
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