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Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides

As an important moiety in natural products, N,O-acetal has attracted wide attention in the past few years. An efficient method to construct N,O-acetal has been developed. Using silver catalyst, cyclobutenediones were smoothly converted to the corresponding γ-aminobutenolides in the presence of forma...

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Autores principales: Wang, Pengcheng, Yu, Ruirui, Ali, Sajjad, Wang, Zhengshen, Liu, Zhigang, Gao, Jinming, Zheng, Huaiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156422/
https://www.ncbi.nlm.nih.gov/pubmed/34067793
http://dx.doi.org/10.3390/molecules26102974
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author Wang, Pengcheng
Yu, Ruirui
Ali, Sajjad
Wang, Zhengshen
Liu, Zhigang
Gao, Jinming
Zheng, Huaiji
author_facet Wang, Pengcheng
Yu, Ruirui
Ali, Sajjad
Wang, Zhengshen
Liu, Zhigang
Gao, Jinming
Zheng, Huaiji
author_sort Wang, Pengcheng
collection PubMed
description As an important moiety in natural products, N,O-acetal has attracted wide attention in the past few years. An efficient method to construct N,O-acetal has been developed. Using silver catalyst, cyclobutenediones were smoothly converted to the corresponding γ-aminobutenolides in the presence of formamides, in which cyclobutenediones likely proceed with a key decarbonylative [3 + 2] cycloaddition process. In this way, a series of products with varied substituents were isolated in moderate yield and fully characterized.
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spelling pubmed-81564222021-05-28 Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides Wang, Pengcheng Yu, Ruirui Ali, Sajjad Wang, Zhengshen Liu, Zhigang Gao, Jinming Zheng, Huaiji Molecules Article As an important moiety in natural products, N,O-acetal has attracted wide attention in the past few years. An efficient method to construct N,O-acetal has been developed. Using silver catalyst, cyclobutenediones were smoothly converted to the corresponding γ-aminobutenolides in the presence of formamides, in which cyclobutenediones likely proceed with a key decarbonylative [3 + 2] cycloaddition process. In this way, a series of products with varied substituents were isolated in moderate yield and fully characterized. MDPI 2021-05-17 /pmc/articles/PMC8156422/ /pubmed/34067793 http://dx.doi.org/10.3390/molecules26102974 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Pengcheng
Yu, Ruirui
Ali, Sajjad
Wang, Zhengshen
Liu, Zhigang
Gao, Jinming
Zheng, Huaiji
Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides
title Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides
title_full Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides
title_fullStr Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides
title_full_unstemmed Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides
title_short Silver Catalyzed Decarbonylative [3 + 2] Cycloaddition of Cyclobutenediones and Formamides
title_sort silver catalyzed decarbonylative [3 + 2] cycloaddition of cyclobutenediones and formamides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156422/
https://www.ncbi.nlm.nih.gov/pubmed/34067793
http://dx.doi.org/10.3390/molecules26102974
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