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Electrochemical C-H arylation of heteroarenes with in situ diazotizated anilines

Zhen-Xiang Liu 1
Zhen-Xiang Liu
, 
Hui Mao 1
Hui Mao
, 
Hang-Cheng Ni 1
Hang-Cheng Ni
, 
Tai-Jin Chen 1
Tai-Jin Chen
1 College of Pharmaceutics, Jinhua Polytechnic, Jinhua, P.R. China
10.1016/j.mencom.2024.06.036
Published 2024-06-19
Communication , Volume 34, Issue 4, 579-580
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Liu Z. et al. Electrochemical C-H arylation of heteroarenes with in situ diazotizated anilines // Mendeleev Communications. 2024. Vol. 34. No. 4. pp. 579-580.
GOST all authors (up to 50) Copy
Liu Z., Mao H., Ni H., Chen T. Electrochemical C-H arylation of heteroarenes with in situ diazotizated anilines // Mendeleev Communications. 2024. Vol. 34. No. 4. pp. 579-580.
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TY - JOUR
DO - 10.1016/j.mencom.2024.06.036
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2024.06.036
TI - Electrochemical C-H arylation of heteroarenes with in situ diazotizated anilines
T2 - Mendeleev Communications
AU - Liu, Zhen-Xiang
AU - Mao, Hui
AU - Ni, Hang-Cheng
AU - Chen, Tai-Jin
PY - 2024
DA - 2024/06/19
PB - Mendeleev Communications
SP - 579-580
IS - 4
VL - 34
ER -
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@article{2024_Liu,
author = {Zhen-Xiang Liu and Hui Mao and Hang-Cheng Ni and Tai-Jin Chen},
title = {Electrochemical C-H arylation of heteroarenes with in situ diazotizated anilines},
journal = {Mendeleev Communications},
year = {2024},
volume = {34},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2024.06.036},
number = {4},
pages = {579--580},
doi = {10.1016/j.mencom.2024.06.036}
}
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Liu, Zhen-Xiang, et al. “Electrochemical C-H arylation of heteroarenes with in situ diazotizated anilines.” Mendeleev Communications, vol. 34, no. 4, Jun. 2024, pp. 579-580. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2024.06.036.

Keywords

anilines
C–H arylation
electrochemical synthesis
heteroarenes
tert-butyl nitrite.

Abstract

A simple and efficient electrochemical C-H arylation of five- membered active heteroarenes involves the application of arenediazonium salts generated in situ from anilines and tert- butyl nitrite. A cathodic reduction-induced radical chain mechanism is proposed.

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