Takizawa Shinobu, Gröger Harald, Sasai Hiroaki
The Institute of Scientific and Industrial Research (ISIR), Osaka University, Mihogaoka, Ibaraki-shi, Osaka 567-0047 (Japan).
Faculty of Chemistry, Bielefeld University, Universitätsstr. 25, 33615 Bielefeld (Germany).
Chemistry. 2015 Jun 15;21(25):8992-7. doi: 10.1002/chem.201406444. Epub 2015 Mar 25.
In recent years vanadium catalysis has been extended to a range of different and even complementary directions in asymmetric synthesis. Inspired by nature's way to activate both substrate and reagent in many cases, the design of efficient bifunctional and dinuclear vanadium catalysts has been achieved. Furthermore, vanadium catalysis has been an early field in which "hybrid catalysts" have been studied in detail by incorporation of oxovanadium complexes into proteins, thus giving artificial enzymes. In addition, a high compatibility of vanadium with proteins enabled the use of vanadium chemocatalysts for combinations with enzyme catalysis in one-pot, thus leading to dynamic kinetic resolutions. In this contribution, these three concepts of vanadium catalysis opening up new perspectives for asymmetric synthesis are reviewed.
近年来,钒催化已扩展到不对称合成中的一系列不同甚至互补的方向。受自然界在许多情况下同时激活底物和试剂方式的启发,已实现了高效双功能和双核钒催化剂的设计。此外,钒催化是一个早期领域,通过将氧钒配合物引入蛋白质中,对“杂化催化剂”进行了详细研究,从而得到人工酶。此外,钒与蛋白质的高度兼容性使得钒化学催化剂能够与酶催化在一锅反应中结合使用,从而实现动态动力学拆分。在本论文中,对钒催化为不对称合成开辟新前景的这三个概念进行了综述。