Thioether-Assisted Cu-Catalyzed C5–H Arylation of Imidazo[1,5-a]pyridines
Author:
Affiliation:
1. Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu, Sichuan 610064, People’s Republic of China
Funder
Central University Basic Research Fund of China
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c01404
Reference43 articles.
1. Imidazo[1,5-a]pyridine derivatives: useful, luminescent and versatile scaffolds for different applications
2. Computational and Spectroscopic Studies of New Rhenium(I) Complexes Containing Pyridylimidazo[1,5-a]pyridine Ligands: Charge Transfer and Dual Emission by Fine-Tuning of Excited States
3. Cationic Heteroleptic Cyclometalated Iridium Complexes with 1-Pyridylimidazo[1,5-α]pyridine Ligands: Exploitation of an Efficient Intersystem Crossing
4. Imidazo[1,5-a]pyridine: A Versatile Architecture for Stable N-Heterocyclic Carbenes
5. Imidazo[1,5-a]pyridine-3-ylidenes—pyridine derived N-heterocyclic carbene ligands
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3. Construction of a Bifunctional Pd(0)‐CALB@SiO2 Hybrid Catalyst for the Synthesis and Arylation of Imidazo[1,2‐a]pyridine in One Pot;European Journal of Organic Chemistry;2023-02-16
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