Zhang Xiaoke
School of Preclinical Medicine, Zunyi Medical University, Zunyi 563006, China.
Institute of Life Sciences, Zunyi Medical University, Zunyi 563006, China.
Molecules. 2024 Oct 14;29(20):4861. doi: 10.3390/molecules29204861.
The metathesis reaction between carbonyl compounds and olefins has emerged as a potent strategy for facilitating swift functional group interconversion and the construction of intricate organic structures through the creation of novel carbon-carbon double bonds. To date, significant progress has been made in carbonyl-olefin metathesis reactions, where oxetane, pyrazolidine, 1,3-diol, and metal alkylidene have been proved to be key intermediates. Recently, several reviews have been disclosed, focusing on distinct catalytic approaches for achieving carbonyl-olefin metathesis. However, the summarization of cyclization strategies for constructing aromatic heterocyclic frameworks through carbonyl-olefin metathesis reactions has rarely been reported. Consequently, we present an up-to-date review of the cyclization strategies in carbonyl-olefin metathesis, categorizing them into three main groups: the formation of monocyclic compounds, bicyclic compounds, and polycyclic compounds. This review delves into the underlying mechanism, scope, and applications, offering a comprehensive perspective on the current strength and the limitation of this field.
羰基化合物与烯烃之间的复分解反应已成为一种有效的策略,可通过形成新的碳-碳双键来促进快速的官能团相互转化以及构建复杂的有机结构。迄今为止,羰基-烯烃复分解反应已取得显著进展,其中氧杂环丁烷、吡唑烷、1,3-二醇和金属亚烷基已被证明是关键中间体。最近,已经发表了几篇综述,重点关注实现羰基-烯烃复分解的不同催化方法。然而,通过羰基-烯烃复分解反应构建芳族杂环骨架的环化策略的总结很少被报道。因此,我们对羰基-烯烃复分解中的环化策略进行了最新综述,将其分为三大类:单环化合物、双环化合物和多环化合物的形成。本综述深入探讨了其潜在机制、范围和应用,对该领域目前的优势和局限性提供了全面的视角。