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
相关论文
共 432 条
[11]   Enantioselective direct α-alkylation of cyclic ketones by means of photo-organocatalysis [J].
Arceo, Elena ;
Bahamonde, Ana ;
Bergonzini, Giulia ;
Melchiorre, Paolo .
CHEMICAL SCIENCE, 2014, 5 (06) :2438-2442
[12]  
Arceo E, 2013, NAT CHEM, V5, P750, DOI [10.1038/NCHEM.1727, 10.1038/nchem.1727]
[13]   ACTIVATION AND REACTION VOLUMES IN SOLUTION [J].
ASANO, T ;
LENOBLE, J .
CHEMICAL REVIEWS, 1978, 78 (04) :407-489
[14]   Microenvironmental polarity control of electron-transfer photochirogenesis. Enantiodifferentiating polar addition of 1,1-diphenyl-1-alkenes photosensitized by saccharide naphthalenecarboxylates [J].
Asaoka, S ;
Wada, T ;
Inoue, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (10) :3008-3027
[15]   Enantiodifferentiating photocyclodimerization of cyclohexa-1,3-diene sensitized by chiral arenecarboxylates [J].
Asaoka, S ;
Ooi, M ;
Jiang, PY ;
Wada, T ;
Inoue, Y .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 2000, (01) :77-84
[16]   Enantiodifferentiating anti-Markovnikov photoaddition of alcohols to 1,1-diphenylalkenes sensitized by chiral naphthalenecarboxylates [J].
Asaoka, S ;
Kitazawa, T ;
Wada, T ;
Inoue, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (37) :8486-8498
[17]  
Asaoka S, 2000, J CHEM SOC PERK T 2, V4, P737
[18]   Intramolecular [2+2] Photocycloaddition of Substituted Isoquinolones: Enantioselectivity and Kinetic Resolution Induced by a Chiral Template [J].
Austin, Kerrie A. B. ;
Herdtweck, Eberhardt ;
Bach, Thorsten .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (36) :8416-8419
[19]   Fun with Photons: Selective Light Induced Reactions in Solution and in Water Soluble Nano-containers [J].
Ayitou, Anoklase ;
Pemberton, Barry C. ;
Kumarasamy, Elango ;
Vallavoju, Nandini ;
Sivaguru, J. .
CHIMIA, 2011, 65 (04) :202-209
[20]   Intermolecular hydrogen binding of a chiral host and a prochiral imidazolidinone:: enantioselective Norrish-Yang cyclisation in solution [J].
Bach, T ;
Aechtner, T ;
Neumüller, B .
CHEMICAL COMMUNICATIONS, 2001, (07) :607-608