Doll Julianna S, Becker Felix J, Roşca Dragoş-Adrian
Anorganisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 276, 69120 Heidelberg, Germany.
ACS Org Inorg Au. 2023 Oct 23;4(1):41-58. doi: 10.1021/acsorginorgau.3c00048. eCollection 2024 Feb 7.
Pyridine is a ubiquitous building block for the design of very diverse ligand platforms, many of which have become indispensable for catalytic transformations. Nevertheless, the isosteric pyrazine, pyrimidine, and triazine congeners have enjoyed thus far a less privileged role in ligand design. In this review, several applications of such fragments in the design of new catalysts are presented. In a significant number of cases described, diazine- and triazine-based ligands either outperform their pyridine congeners or offer alternative catalytic pathways which enable new reactivities. The potential opportunities unlocked by using these building blocks in ligand design are discussed, and the origin of the enhanced catalytic activity is highlighted where mechanistic studies are available.
吡啶是设计多种多样配体平台的一种普遍存在的结构单元,其中许多配体平台已成为催化转化中不可或缺的部分。然而,等电子体吡嗪、嘧啶和三嗪同系物在配体设计中迄今所起的作用相对较小。在本综述中,介绍了这些片段在新型催化剂设计中的几种应用。在所描述的大量案例中,基于二嗪和三嗪的配体要么优于它们的吡啶同系物,要么提供了能够实现新反应活性的替代催化途径。讨论了在配体设计中使用这些结构单元所带来的潜在机遇,并在有机理研究的情况下强调了催化活性增强的根源。