Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, West China Medical School, Sichuan University, 29 Wangjiang Road, Chengdu 610064, PR China.
Chemistry. 2011 May 9;17(20):5466-92. doi: 10.1002/chem.201003039. Epub 2011 Apr 19.
The biheteroaryl structural motif is prevalent in polymers, advanced materials, liquid crystals, ligands, molecules of medicinal interest, and natural products. Many types of synthetic transformations have been known for the construction of heteroaryl-heteroaryl linkages. Coupling reactions provide one of the most efficient ways to achieve these biheterocyclic structures. In this review, four types of coupling reactions are discussed: 1) transition-metal-catalyzed coupling reactions of heteroaryl halides or surrogates with heteroarylmetals; 2) direct inter- and intramolecular heteroarylations of C sp 2-H bonds of heteroarenes with heteroaryl halides or pseudohalides; 3) oxidative C-H/C-H homo- and cross-couplings of two unpreactivated heteroarenes; and 4) transition-metal-catalyzed decarboxylative cross-coupling reactions between haloheteroarenes or heteroarenes and heteroarenecarboxylic acids. The general purpose of this review is to give an exhaustive and clear picture in heteroaryl-heteroaryl bond formation as well as its application in the synthesis of natural products, pharmaceuticals, catalyst ligands, and materials.
双杂芳基结构基序在聚合物、先进材料、液晶、配体、具有药用价值的分子和天然产物中很常见。已经有许多类型的合成转化方法用于构建杂芳基-杂芳基键。偶联反应是实现这些双杂环结构的最有效方法之一。在这篇综述中,讨论了四种类型的偶联反应:1)杂芳基卤化物或前体与杂芳基金属的过渡金属催化偶联反应;2)杂芳基卤化物或拟卤化物与杂芳基 Csp2-H 键的直接分子间和分子内杂芳基化;3)两个未活化杂芳烃的氧化 C-H/C-H 同系物和交叉偶联;4)卤代杂芳基或杂芳烃与杂芳基羧酸之间的过渡金属催化脱羧交叉偶联反应。本综述的一般目的是全面而清晰地描述杂芳基-杂芳基键的形成,以及其在天然产物、药物、催化剂配体和材料合成中的应用。