Palladium-Catalyzed Denitrative α-Arylation of Heteroarenes with Nitroarenes via C–H and C–NO<sub>2</sub> Bond Activations-Reference-Cited by-同舟云学术

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Palladium-Catalyzed Denitrative α-Arylation of Heteroarenes with Nitroarenes via C–H and C–NO₂ Bond Activations

Published:2024-08-22 Issue:35 Volume:26 Page:7307-7312
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yao Jiaxin¹,Xiao Yuxuan¹,Li Haiyan¹,Yang Xun¹,Du Jiahui¹,Yin Ying¹,Feng Lin¹,Duan Wengui¹^ORCID,Yu Lin¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, Guangxi University, Nanning 530004, Guangxi, P. R. China

Funder

Guangxi University

Specific Research Project of Guangxi for Research Bases and Talents

Natural Science Foundation of Guangxi Zhuang Autonomous Region

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02340

Reference50 articles.

1. 2-Arylbenzofuran, Flavonoid, and Tyrosinase Inhibitory Constituents of Morus yunnanensis

2. Rings in Drugs

3. Turning on the solid emission from non-emissive 2-aryl-3-cyanobenzofurans by tethering tetraphenylethene for green electroluminescence

4. From Nature to Drug Discovery: The Indole Scaffold as a ‘Privileged Structure’

5. The Azaindole Framework in the Design of Kinase Inhibitors

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