Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States.
Chem Rev. 2022 Jan 26;122(2):1654-1716. doi: 10.1021/acs.chemrev.1c00467. Epub 2021 Oct 4.
Asymmetric catalysis is a major theme of research in contemporary synthetic organic chemistry. The discovery of general strategies for highly enantioselective photochemical reactions, however, has been a relatively recent development, and the variety of photoreactions that can be conducted in a stereocontrolled manner is consequently somewhat limited. Asymmetric photocatalysis is complicated by the short lifetimes and high reactivities characteristic of photogenerated reactive intermediates; the design of catalyst architectures that can provide effective enantiodifferentiating environments for these intermediates while minimizing the participation of uncontrolled racemic background processes has proven to be a key challenge for progress in this field. This review provides a summary of the chiral catalyst structures that have been studied for solution-phase asymmetric photochemistry, including chiral organic sensitizers, inorganic chromophores, and soluble macromolecules. While some of these photocatalysts are derived from privileged catalyst structures that are effective for both ground-state and photochemical transformations, others are structural designs unique to photocatalysis and offer insight into the logic required for highly effective stereocontrolled photocatalysis.
不对称催化是当代合成有机化学的一个主要研究课题。然而,通用的高对映选择性光化学反应策略的发现是相对较新的发展,因此能够以立体控制方式进行的光反应的种类有些有限。不对称光催化由于光生反应中间体的寿命短和反应性高而变得复杂;设计能够为这些中间体提供有效区分对映体的环境,同时最小化不受控制的外消旋背景过程参与的催化剂结构已被证明是该领域取得进展的关键挑战。本综述提供了用于溶液相不对称光化学的手性催化剂结构的总结,包括手性有机敏化剂、无机生色团和可溶性聚合物。虽然其中一些光催化剂源自对基态和光化学转化均有效的特权催化剂结构,但其他结构设计是光催化特有的,为高效立体控制光催化所需的逻辑提供了见解。