Investigating catalytic pathways: a comparative review of homogeneous and heterogeneous catalysis for 3-aroylimidazo[1,2-a]pyridine synthesis-Reference-Cited by-同舟云学术

Investigating catalytic pathways: a comparative review of homogeneous and heterogeneous catalysis for 3-aroylimidazo[1,2-a]pyridine synthesis

Published:2023-12-03 Issue: Volume: Page:
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Moutaouakil Mohamed,Roby Othmane,Tighadouini Said,Cherif Abdelmjid,El Aatiaoui Abdelmalik,Saddik Rafik

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s11030-023-10765-w.pdf

Reference45 articles.

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2. Hong B, Lin B, Yao Y et al (2022) Synthesis of 3-substituted 2-trifluomethyl imidazo[1,2-a]pyridine through [3+2] cycloaddition of pyridinium ylide with trifluoroacetonitrile. Tetrahedron Lett 111:154206. https://doi.org/10.1016/j.tetlet.2022.154206

3. Shi L, Li T, Mei G-J (2022) Recent advances in transition-metal-free C-H functionalization of imidazo[1,2-a]pyridines. Green Synthesis Catal 3:227–242. https://doi.org/10.1016/j.gresc.2022.03.007

4. Salamatmanesh A, Heydari A (2021) Magnetic nanostructure-anchored mixed-donor ligand system based on carboxamide and N-heterocyclic thiones: an efficient support of CuI catalyst for synthesis of imidazo[1,2-a]pyridines in eutectic medium. Appl Catal A 624:118306. https://doi.org/10.1016/j.apcata.2021.118306

5. Kawakubo M, Inaguma Y, Murata Y et al (2022) Synthesis of novel 5-iodopyrido[1′,2′;2,3]imidazo[5,1-a]isoquinolinium iodides from 2-(2-ethynylphenyl)imidazo[1,2-a]pyridines via iodocyclization. Tetrahedron Lett 105:154054. https://doi.org/10.1016/j.tetlet.2022.154054

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