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Synthesis of Phenol-Pyridinium Salts Enabled by Tandem Electron Donor-Acceptor Complexation and Iridium Photocatalysis
被引:5
|作者:
Carson, Matthew C.
[1
]
Liu, Cindy R.
[1
]
Kozlowski, Marisa C.
[1
]
机构:
[1] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
来源:
关键词:
C-H AMINATION;
REACTIVITY;
FUNCTIONALIZATION;
AMINES;
MODEL;
RING;
D O I:
10.1021/acs.joc.3c02872
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Herein, we describe a dual photocatalytic system to synthesize phenol-pyridinium salts using visible light. Utilizing both electron donor-acceptor (EDA) complex and iridium(III) photocatalytic cycles, the C-N cross-coupling of unprotected phenols and pyridines proceeds in the presence of oxygen to furnish pyridinium salts. Photocatalytic generation of phenoxyl radical cations also enabled a nucleophilic aromatic substitution (SNAr) of a fluorophenol with an electron-poor pyridine. Spectroscopic experiments were conducted to probe the mechanism and reaction selectivity. The unique reactivity of these phenol-pyridinium salts were displayed in several derivatization reactions, providing rapid access to a diverse chemical space.
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页码:3419 / 3429
页数:11
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