The Department of Chemistry, The University of British Columbia, 2036 Main Mall, Vancouver, BC, CanadaV6K 1X8.
Chem Soc Rev. 2020 Oct 5;49(19):6947-6994. doi: 10.1039/d0cs00229a.
Titanium is the second most abundant transition metal and is already a key player in important industrial processes (e.g. polyethylene). Titanium is an attractive metal to use for catalytic transformations as it is a versatile and inexpensive metal of low-toxicity and of established biocompatibility. However, its potential use as a catalyst for the synthesis of fine chemicals, pharmaceuticals and agrochemicals is often overlooked due to its oxophilic, Lewis acidic character, which renders complexes of titanium less functional group tolerant than their late transition metal counterparts. Nevertheless, three different fields of research in titanium catalysis have drawn attention in recent years: formal redox catalysis, hydroamination and hydroaminoalkylation. For these reactions, titanium offers new approaches and alternative pathways/mechanisms that are complementary to late transition metal-based catalysis. This review focuses on advances in fine chemical synthesis by titanium-catalyzed reactions featuring redox transformations and two important hydrofunctionalization reactions, hydroamination and hydroaminoalkylation. Starting from the late 90s, we provide an overview of historic inspirational contributions, both catalytic and stoichiometric, and the latest insights in catalyst design efforts, mechanistic details and utility of the three different classes of transformations. Insights to enhance catalyst activity as well as catalyst controlled regio- and stereoselectivities are presented. Illustrative examples that highlight substrate scope and the application of titanium catalysis to the synthesis of complex organic small molecules, natural products and materials are shown. Finally, opportunities and strategies for on-going research and development activities in titanium catalysis are highlighted.
钛是第二丰富的过渡金属,已经是重要工业过程(例如聚乙烯)中的关键角色。钛是一种用于催化转化的有吸引力的金属,因为它是一种多功能、廉价、低毒性且具有既定生物相容性的金属。然而,由于其亲氧性和路易斯酸性,钛的潜在用途作为精细化学品、药物和农用化学品合成的催化剂往往被忽视,这使得钛配合物对功能基团的耐受性不如其后过渡金属对应物。尽管如此,近年来钛催化的三个不同研究领域引起了关注:形式氧化还原催化、氨氢化和氨烷基化。对于这些反应,钛提供了新的方法和替代途径/机制,与后过渡金属催化互补。
本综述重点介绍了通过钛催化的具有氧化还原转化和两个重要的氢官能化反应(氨氢化和氨烷基化)的精细化学品合成方面的进展。从 90 年代末开始,我们提供了历史性的灵感贡献(包括催化和计量学方面)的概述,以及催化剂设计工作、反应机理细节和三种不同转化类别的实用性的最新见解。介绍了提高催化剂活性以及催化剂控制区域和立体选择性的见解。展示了突出底物范围和钛催化在复杂有机小分子、天然产物和材料合成中的应用的说明性实例。最后,强调了钛催化持续研究和开发活动的机会和策略。