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Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed Three-Component Reaction under Microwave Irradiation
[Image: see text] An expeditious one-pot, ligand-free, Pd(OAc)(2)-catalyzed, three-component reaction for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines was developed under microwave irradiation. With the high availability of commercial reagents and great efficiency in expanding molecule diversi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059256/ https://www.ncbi.nlm.nih.gov/pubmed/24854606 http://dx.doi.org/10.1021/ol501136e |
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author | Wang, Yuanxiang Frett, Brendan Li, Hong-yu |
author_facet | Wang, Yuanxiang Frett, Brendan Li, Hong-yu |
author_sort | Wang, Yuanxiang |
collection | PubMed |
description | [Image: see text] An expeditious one-pot, ligand-free, Pd(OAc)(2)-catalyzed, three-component reaction for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines was developed under microwave irradiation. With the high availability of commercial reagents and great efficiency in expanding molecule diversity, this methodology is superior to the existing procedures for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines analogues. |
format | Online Article Text |
id | pubmed-4059256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40592562015-05-22 Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed Three-Component Reaction under Microwave Irradiation Wang, Yuanxiang Frett, Brendan Li, Hong-yu Org Lett [Image: see text] An expeditious one-pot, ligand-free, Pd(OAc)(2)-catalyzed, three-component reaction for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines was developed under microwave irradiation. With the high availability of commercial reagents and great efficiency in expanding molecule diversity, this methodology is superior to the existing procedures for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines analogues. American Chemical Society 2014-05-22 2014-06-06 /pmc/articles/PMC4059256/ /pubmed/24854606 http://dx.doi.org/10.1021/ol501136e Text en Copyright © 2014 American Chemical Society |
spellingShingle | Wang, Yuanxiang Frett, Brendan Li, Hong-yu Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed Three-Component Reaction under Microwave Irradiation |
title | Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed
Three-Component Reaction under Microwave Irradiation |
title_full | Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed
Three-Component Reaction under Microwave Irradiation |
title_fullStr | Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed
Three-Component Reaction under Microwave Irradiation |
title_full_unstemmed | Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed
Three-Component Reaction under Microwave Irradiation |
title_short | Efficient Access to 2,3-Diarylimidazo[1,2-a]pyridines via a One-Pot, Ligand-Free, Palladium-Catalyzed
Three-Component Reaction under Microwave Irradiation |
title_sort | efficient access to 2,3-diarylimidazo[1,2-a]pyridines via a one-pot, ligand-free, palladium-catalyzed
three-component reaction under microwave irradiation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059256/ https://www.ncbi.nlm.nih.gov/pubmed/24854606 http://dx.doi.org/10.1021/ol501136e |
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