Visible-light-mediated C–H amidation of imidazoheterocycles with <i>N</i>-amidopyridiniums-Reference-Cited by-同舟云学术

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Visible-light-mediated C–H amidation of imidazoheterocycles with N-amidopyridiniums

Published:2024 Issue:23 Volume:22 Page:4647-4650
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wen Lili¹,Tan Qiannan¹,Pi Chao²^ORCID,Yuan Juan¹^ORCID,Zhang Jingyu¹,Mi Xia¹^ORCID

Affiliation:

1. College of Pharmacy, Henan University of Chinese Medicine, Zhengzhou 450046, China

2. Henan Key Laboratory of Chemical Biology and Organic Chemistry, Key Laboratory of Applied Chemistry of Henan Universities, Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou 450052, China

Abstract

C-3 amidated imidazoheterocycles were synthesized via a visible light-promoted reaction of imidazoheterocycles with N-amidopyridinium salts catalyzed by 4CzIPN under mild conditions.

Funder

Education Department of Henan Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00461B

Reference27 articles.

1. Recent Progress in the Pharmacology of Imidazo[1,2-a]pyridines

2. Synthesis and antiprotozoal activity of novel bis-benzamidino imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines

3. Design and Synthesis of Imidazopyridine Analogues as Inhibitors of Phosphoinositide 3-Kinase Signaling and Angiogenesis

4. Imidazo[1,2-a]pyridines Susceptible to Excited State Intramolecular Proton Transfer: One-Pot Synthesis via an Ortoleva–King Reaction

5. Antibacterial activities of Groebke–Blackburn–Bienaymé-derived imidazo[1,2-a]pyridin-3-amines

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