Alkoxy Radicals See the Light: New Paradigms of Photochemical Synthesis

被引:298
作者
Chang, Liang [1 ,2 ]
An, Qing [3 ]
Duan, Lingfei [1 ]
Feng, Kaixuan [1 ]
Zuo, Zhiwei [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Peoples R China
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
BOND-DISSOCIATION ENERGIES; HYDROGEN-ATOM TRANSFER; COUPLED ELECTRON-TRANSFER; C-H BONDS; CYCLOBUTANOLS REGIOSPECIFIC SYNTHESIS; TRANSITION-METAL-COMPLEXES; RING-OPENING CHLORINATION; ABSOLUTE RATE CONSTANTS; LASER FLASH-PHOTOLYSIS; MEDIUM-SIZED LACTONES;
D O I
10.1021/acs.chemrev.1c00256
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alkoxy radicals are highly reactive species that have long been recognized as versatile intermediates in organic synthesis. However, their development has long been impeded due to a lack of convenient methods for their generation. Thanks to advances in photoredox catalysis, enabling facile access to alkoxy radicals from bench-stable precursors and free alcohols under mild conditions, research interest in this field has been renewed. This review comprehensively summarizes the recent progress in alkoxy radical-mediated transformations under visible light irradiation. Elementary steps for alkoxy radical generation from either radical precursors or free alcohols are central to reaction development; thus, each section is categorized and discussed accordingly. Throughout this review, we have focused on the different mechanisms of alkoxy radical generation as well as their impact on synthetic utilizations. Notably, the catalytic generation of alkoxy radicals from abundant alcohols is still in the early stage, providing intriguing opportunities to exploit alkoxy radicals for diverse synthetic paradigms.
引用
收藏
页码:2429 / 2486
页数:58
相关论文
共 344 条
[1]   Energy Read-out as a Probe of Kinetically Hidden Transition States [J].
Alvi, Scheherzad ;
Singleton, Daniel A. .
ORGANIC LETTERS, 2021, 23 (06) :2174-2177
[2]   Cerium-Catalyzed C-H Functionalizations of Alkanes Utilizing Alcohols as Hydrogen Atom Transfer Agents [J].
An, Qing ;
Wang, Ziyu ;
Chen, Yuegang ;
Wang, Xin ;
Zhang, Kaining ;
Pan, Hui ;
Liu, Weimin ;
Zuo, Zhiwei .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (13) :6216-6226
[3]   REACTION OF ATOMIC OXYGEN WITH SOME SIMPLE ALKENES .2. REACTION PATHWAYS INVOLVING ETHENE, PROPENE AND (E)-BUT-2-ENE AT ATMOSPHERIC-PRESSURE [J].
ANASTASI, C ;
SANDERSON, MG ;
PAGSBERG, P ;
SILLESEN, A .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1994, 90 (24) :3625-3631
[4]   Gas-phase acidities and O-H bond dissociation enthalpies of phenol, 3-methylphenol, 2,4,6-trimethylphenol, and ethanoic acid [J].
Angel, Laurence A. ;
Ervin, Kent M. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (35) :10392-10403
[5]   Photoredox-Catalyzed Site-Selective α-C(sp3)-H Alkylation of Primary Amine Derivatives [J].
Ashley, Melissa A. ;
Yamauchi, Chiaki ;
Chu, John C. K. ;
Otsuka, Shinya ;
Yorimitsu, Hideki ;
Rovis, Tomislav .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (12) :4002-4006
[6]   Atmospheric degradation of volatile organic compounds [J].
Atkinson, R ;
Arey, J .
CHEMICAL REVIEWS, 2003, 103 (12) :4605-4638
[7]   POLAR AND SOLVENT EFFECTS IN CLEAVAGE OF T-ALKOXY RADICALS [J].
BACHA, JD ;
KOCHI, JK .
JOURNAL OF ORGANIC CHEMISTRY, 1965, 30 (10) :3272-&
[8]   Spectral properties and absolute rate constants for ß-scission of ring-substituted cumyloxyl radicals.: A laser flash photolysis study [J].
Baciocchi, E ;
Bietti, M ;
Salamone, M ;
Steenken, S .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (07) :2266-2270
[9]   Oxygen acidity of 1-arylalkanol radical cations.: 4-methoxycumyloxyl radical as -C(Me)2-O--to-nucleus electron-transfer intermediate in the reaction of 4-methoxycumyl alcohol radical cation with OH- [J].
Baciocchi, E ;
Bietti, M ;
Lanzalunga, O ;
Steenken, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (44) :11516-11517
[10]   Base-catalyzed C-H deprotonation of 4-methoxybenzyl alcohol radical cations in water: Evidence for a carbon-to-oxygen 1,2-H-shift mechanism [J].
Baciocchi, E ;
Bietti, M ;
Steenken, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (17) :4078-4079