Tetrahedron letters2022，Vol.1023.DOI:10.1016/j.tetlet.2022.153920

Transtion-metal-free access to 2-arylphenethylamines through aryldiazonium ion catalyzed ring-opening of aziridines with arenes

Feng, Yunqiu Huai, Menglin Huang, Tian Gao, Minghui Tao, Chuanzhou
Tetrahedron letters2022，Vol.1023.DOI:10.1016/j.tetlet.2022.153920
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  • NSTL
  • Elsevier

Transtion-metal-free access to 2-arylphenethylamines through aryldiazonium ion catalyzed ring-opening of aziridines with arenes

Feng, Yunqiu 1Huai, Menglin 1Huang, Tian 1Gao, Minghui 1Tao, Chuanzhou1
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作者信息

  • 1. Jiangsu Ocean Univ
  • 折叠

Abstract

Aryldiazonium ions have been proven to catalyze effective cleavage of aziridines for the installation of varied aryl groups, providing access to a variety of 2-arylphenethylamines. This highly regioselective pro-cess, which can be performed at gram-scale, enjoys operational simplicity, as well as mild and metal-free conditions.(c) 2022 Elsevier Ltd. All rights reserved.

Key words

Aryldiazonium ion/Aziridine/2-Arylphenethylamine/Transition -metal -free/C-ARYLATION/EFFICIENT CATALYST/LEWIS-ACID/PHOTOREDOX/NITROALKENES/VERSATILE

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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38
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