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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8156422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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