Nájera Carmen, Beletskaya Irina P, Yus Miguel
Centro de Innovación en Química Avanzada (ORFEO-CINQA), Universidad de Alicante, Apdo. 99, E-03080 Alicante, Spain.
Chem Soc Rev. 2019 Aug 12;48(16):4515-4618. doi: 10.1039/c8cs00872h.
Metal-catalyzed regiodivergent reactions allow control over regioselectivity in the synthesis of a wide range of organic products. Starting from the same material, it is possible to prepare different regioisomers just by appropriately choosing the catalyst or by modifying the reaction conditions. Therefore, these regiodivergent methodologies should be included as the key factor in the concept of efficiency and atom economy in synthetic organic chemistry. The synthetic potential of this subject has been demonstrated mainly in addition reactions to unsaturated carbon-carbon bonds, allylic and propargylic nucleophilic substitutions, C-H activation reactions, cross-couplings, and intramolecular or intermolecular cyclizations. This review article overviews the development and rationalization of regiodivergence in these fundamental reactions in the last 15 years.
金属催化的区域发散反应能够控制多种有机产物合成中的区域选择性。从相同的原料出发,仅通过适当地选择催化剂或改变反应条件,就有可能制备不同的区域异构体。因此,这些区域发散方法应被视为合成有机化学中效率和原子经济性概念的关键因素。该领域的合成潜力主要体现在对不饱和碳 - 碳键的加成反应、烯丙基和亲丙基亲核取代反应、C - H活化反应、交叉偶联反应以及分子内或分子间环化反应中。这篇综述文章概述了过去15年中这些基本反应中区域发散性的发展与合理性。