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Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction

The unsaturated aza-heterocycles such as tetrahydropyridines pose significant applications in both drug discovery and development. However, the methods to construct polyfunctionalized tetrahydropyridines are still limited. Herein, we report a modular synthesis of tetrahydropyridines via copper catal...

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Detalles Bibliográficos
Autores principales: Wei, Siqi, Zhang, Guocong, Wang, Yahui, You, Mengwei, Wang, Yanan, Zhou, Liejin, Zhang, Zuxiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988680/
https://www.ncbi.nlm.nih.gov/pubmed/36895640
http://dx.doi.org/10.1016/j.isci.2023.106137
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author Wei, Siqi
Zhang, Guocong
Wang, Yahui
You, Mengwei
Wang, Yanan
Zhou, Liejin
Zhang, Zuxiao
author_facet Wei, Siqi
Zhang, Guocong
Wang, Yahui
You, Mengwei
Wang, Yanan
Zhou, Liejin
Zhang, Zuxiao
author_sort Wei, Siqi
collection PubMed
description The unsaturated aza-heterocycles such as tetrahydropyridines pose significant applications in both drug discovery and development. However, the methods to construct polyfunctionalized tetrahydropyridines are still limited. Herein, we report a modular synthesis of tetrahydropyridines via copper catalyzed multicomponent radical cascade reaction. The reaction features mild conditions and broad substrate scope. In addition, the reaction could scale up to gram scale with similar yield. A variety of 1,2,5,6-tetrahydropyridines with C3 and C5 substituents could be assembled from simple starting materials. More importantly, the products could serve as versatile intermediate to access various functionalized aza-heterocycles which further demonstrates its utility.
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spelling pubmed-99886802023-03-08 Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction Wei, Siqi Zhang, Guocong Wang, Yahui You, Mengwei Wang, Yanan Zhou, Liejin Zhang, Zuxiao iScience Article The unsaturated aza-heterocycles such as tetrahydropyridines pose significant applications in both drug discovery and development. However, the methods to construct polyfunctionalized tetrahydropyridines are still limited. Herein, we report a modular synthesis of tetrahydropyridines via copper catalyzed multicomponent radical cascade reaction. The reaction features mild conditions and broad substrate scope. In addition, the reaction could scale up to gram scale with similar yield. A variety of 1,2,5,6-tetrahydropyridines with C3 and C5 substituents could be assembled from simple starting materials. More importantly, the products could serve as versatile intermediate to access various functionalized aza-heterocycles which further demonstrates its utility. Elsevier 2023-02-09 /pmc/articles/PMC9988680/ /pubmed/36895640 http://dx.doi.org/10.1016/j.isci.2023.106137 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wei, Siqi
Zhang, Guocong
Wang, Yahui
You, Mengwei
Wang, Yanan
Zhou, Liejin
Zhang, Zuxiao
Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
title Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
title_full Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
title_fullStr Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
title_full_unstemmed Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
title_short Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
title_sort modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988680/
https://www.ncbi.nlm.nih.gov/pubmed/36895640
http://dx.doi.org/10.1016/j.isci.2023.106137
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