对映选择合成
光催化
化学
发色团
催化作用
组合化学
光化学
纳米技术
有机化学
材料科学
作者
Matthew J. Genzink,Jesse B. Kidd,Wesley B. Swords,Tehshik P. Yoon
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2021-10-04
卷期号:122 (2): 1654-1716
被引量:259
标识
DOI:10.1021/acs.chemrev.1c00467
摘要
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.
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