Tetrahedron letters2022,Vol.994.DOI:10.1016/j.tetlet.2022.153846

Weak Bronsted base-promoted photoredox catalysis for C-H alkylation of heteroarenes mediated by triplet excited diaryl ketone

Li, Lifan Song, Xuyan Qi, Mei-Fang Sun, Bing
Tetrahedron letters2022,Vol.994.DOI:10.1016/j.tetlet.2022.153846

Weak Bronsted base-promoted photoredox catalysis for C-H alkylation of heteroarenes mediated by triplet excited diaryl ketone

Li, Lifan 1Song, Xuyan 2Qi, Mei-Fang 1Sun, Bing1
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作者信息

  • 1. Wuhan Univ Technol
  • 2. China Tobacco Hubei Ind LLC
  • 折叠

Abstract

A weak Bronsted base-promoted photoredox catalysis has been developed for the direct C-H alpha-alkyla-tion of heteroarenes with cyclic and acyclic ethers. The high efficiency of this strategy is demonstrated by the mild reaction conditions, broad substrate scope, economical reagents and high regioselectivity. With air as the sole oxidant, a set of alkylated heteroarenes were accessed smoothly. This strategy was also applied for late-stage functionalization of valuable vitamin E nicotinate and loratadine. (C) 2022 Elsevier Ltd. All rights reserved.

Key words

Photoredox/Br?nsted base/Alkylation/Heteroarene/Diaryl ketone/FREE-RADICAL REACTIONS/N-OXIDES/FUNCTIONALIZATION/ETHERS/ARYLATION/C(SP(3))-H/ACID

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出版年

2022
Tetrahedron letters

Tetrahedron letters

CCR
ISSN:0040-4039
被引量1
参考文献量40
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