State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, University of Chinese Academy of Sciences, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032 China.
School of Chemistry and Molecular Bioscience, Molecular Horizons Research Institute, University of Wollongong,Wollongong New South Wales 2500, Australia.
Chem Rev. 2021 Jul 28;121(14):8685-8755. doi: 10.1021/acs.chemrev.0c00624. Epub 2020 Nov 12.
The past decade has witnessed the golden age of homogeneous gold-catalyzed reactions, especially those that involve the transformation of highly strained molecules into complex molecular architectures. Gold catalysts, with unique electronic properties and catalytic abilities, have elevated versatile reaction modes through π-interaction induced activation. On the basis of increasing research interest in this topic, together with the significant development of various ligands, including phosphine ligands and azacyclic or noncyclic carbene ligands, the understanding of the catalytic function of gold catalysts has become much deeper and more comprehensive. Different reaction needs thus could be adapted by a novel gold catalyst with a diversified ligand selection. Furthermore, the whole evolution of the gold catalysis on synthetic methodologies has realized and expanded its application into natural product synthesis as well as the potentiality of drug discovery, which endows this ancient metal with a magnificent renaissance. The reactivity of strained small ring molecules with high tension has always been an important research topic in organic chemistry. When the highly strained small ring is linked with a π-electron rich moiety or contains a heteroatom, the gold activation of the π-system or coordination with the heteroatom can initiate a cascade reaction, usually followed by ring opening or expansion. These processes can result in the rapid construction of complex and distinct molecular structures, many of which feature in biologically important molecules. In this review, we will mainly summarize the advances on diverse reaction types and molecular constructions accomplished by homogeneous gold catalysis using highly strained substrates, including methylenecyclopropanes (MCPs), vinylidenecyclopropanes (VDCPs), cyclopropenes as well as aziridine- and epoxide-containing molecules, focusing on the last 10 years. For functionalized alkynyl cyclopropanes, several early inspiring and elegant examples will be described in this review for systematically understanding these transformations.
过去十年见证了均相金催化反应的黄金时代,尤其是那些涉及将高度应变分子转化为复杂分子结构的反应。金催化剂具有独特的电子性质和催化能力,通过π-相互作用诱导的活化,提升了多种反应模式。在对这一主题的研究兴趣不断增加的基础上,以及各种配体(包括膦配体和氮杂环卡宾或非环卡宾配体)的显著发展,对金催化剂催化功能的理解变得更加深入和全面。不同的反应需求可以通过新型金催化剂与多样化配体选择来适应。此外,金催化在合成方法上的整体发展已经实现并扩展了其在天然产物合成以及药物发现方面的应用,这赋予了这种古老金属一种壮丽的复兴。具有高张力的小环应变分子的反应性一直是有机化学的一个重要研究课题。当高度应变的小环与π-电子富电子部分相连或含有杂原子时,π-体系的金活化或与杂原子的配位可以引发级联反应,通常伴随着环的打开或扩张。这些过程可以快速构建复杂而独特的分子结构,其中许多具有生物重要的分子。在这篇综述中,我们将主要总结使用高度应变底物通过均相金催化完成的各种反应类型和分子构建的进展,包括亚甲基环丙烷(MCPs)、乙烯基环丙烷(VDCPs)、环丙烯以及含氮杂环丙烷和环氧化物的分子,重点关注过去 10 年的进展。对于功能化炔基环丙烷,本文将描述几个早期的鼓舞人心和优雅的例子,以便系统地理解这些转化。