Recent advances in [2+2+2] cycloaddition reactions

被引:470
|
作者
Dominguez, Gema [1 ]
Perez-Castells, Javier [1 ]
机构
[1] Univ San Pablo CEU, Fac Farm, Dept Quim, Madrid 28668, Spain
关键词
COBALT-CATALYZED CYCLOTRIMERIZATION; N-H ACTIVATION; ENANTIOSELECTIVE SYNTHESIS; REGIOSELECTIVE CYCLOTRIMERIZATION; ALKYNE CYCLOTRIMERIZATION; AXIAL CHIRALITY; C-H; EFFICIENT; ALKENES; CONSTRUCTION;
D O I
10.1039/c1cs15029d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:3430 / 3444
页数:15
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