Chiral Photocatalyst Structures in Asymmetric Photochemical Synthesis

被引:275
作者
Genzink, Matthew J. [1 ]
Kidd, Jesse B. [1 ]
Swords, Wesley B. [1 ]
Yoon, Tehshik P. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
关键词
INTRAMOLECULAR 2+2 PHOTOCYCLOADDITION; LEWIS-ACID CATALYSIS; Z-E PHOTOISOMERIZATION; ANTI-MARKOVNIKOV PHOTOADDITION; DIELS-ALDER REACTION; ENANTIODIFFERENTIATING 4+4 PHOTOCYCLODIMERIZATION; ELECTRON-TRANSFER-REACTIONS; CHARGE-TRANSFER PHENOMENA; HUMAN SERUM-ALBUMIN; DIRECTED ENANTIOSELECTIVE PHOTOCYCLODIMERIZATION;
D O I
10.1021/acs.chemrev.1c00467
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:1654 / 1716
页数:63
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