Departamento de Química, Facultad de Farmacia, Universidad San Pablo-CEU, Boadilla del Monte, 28668-Madrid, Spain.
Chem Soc Rev. 2011 Jul;40(7):3430-44. doi: 10.1039/c1cs15029d. Epub 2011 Mar 23.
The [2+2+2] cycloaddition is an elegant, atom-efficient and group tolerant process for the synthesis of carbo- and heterocycles, mostly aromatic, involving the formation of several C-C bonds in a single step. Cyclotrimerisation is catalyzed by a variety of organometallic complexes, including more than 15 different metals. The aim of this tutorial review is to point out the most recent advances in this field and to encourage the use of this reaction enroute to complex molecules. After summarizing the most common catalysts and reaction conditions generally used, we survey the mechanistic features currently accepted for this reaction. Section 4 covers the scope of the different [2+2+2] cycloaddition versions starting with the cyclotrimerisation of three triple bonds, including nitriles, with especial emphasis on asymmetric reactions that create central, axial or planar chirality. Then, reactions that use double bonds are addressed. Finally, the most outstanding examples of natural products synthesis using [2+2+2] cycloadditions as a key step reported recently are shown.
[2+2+2]环加成是一种优雅、原子经济性和基团耐受性的合成碳环和杂环的方法,主要涉及芳香族化合物,通过一步反应形成多个 C-C 键。环三聚反应由各种有机金属配合物催化,包括超过 15 种不同的金属。本综述的目的是指出该领域的最新进展,并鼓励在合成复杂分子的过程中使用这种反应。在总结了通常使用的最常见的催化剂和反应条件之后,我们研究了目前公认的该反应的机理特征。第 4 节涵盖了不同的[2+2+2]环加成版本的范围,从三个三键的环三聚反应开始,包括腈,特别强调了产生中心、轴向或平面手性的不对称反应。然后,讨论了使用双键的反应。最后,展示了最近报道的使用[2+2+2]环加成作为关键步骤合成天然产物的最杰出例子。