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Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase
During a synthesis of coumarins to obtain new candidates for treating Alzheimer’s Disease (AD), an unusual rearrangement of a benzopyran group to a benzofuran group occurred, offering a novel synthesis pathway of these benzofuran derivatives. The possible mechanism of the novel rearrangement was als...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259253/ https://www.ncbi.nlm.nih.gov/pubmed/21116228 http://dx.doi.org/10.3390/molecules15128593 |
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author | Zhou, Xiang Li, Miao Wang, Xiao-Bing Wang, Tao Kong, Ling-Yi |
author_facet | Zhou, Xiang Li, Miao Wang, Xiao-Bing Wang, Tao Kong, Ling-Yi |
author_sort | Zhou, Xiang |
collection | PubMed |
description | During a synthesis of coumarins to obtain new candidates for treating Alzheimer’s Disease (AD), an unusual rearrangement of a benzopyran group to a benzofuran group occurred, offering a novel synthesis pathway of these benzofuran derivatives. The possible mechanism of the novel rearrangement was also discussed. All of the benzofuran derivatives have weak anti-AChE activities compared with the reference compound, donepezil. |
format | Online Article Text |
id | pubmed-6259253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62592532018-12-06 Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase Zhou, Xiang Li, Miao Wang, Xiao-Bing Wang, Tao Kong, Ling-Yi Molecules Article During a synthesis of coumarins to obtain new candidates for treating Alzheimer’s Disease (AD), an unusual rearrangement of a benzopyran group to a benzofuran group occurred, offering a novel synthesis pathway of these benzofuran derivatives. The possible mechanism of the novel rearrangement was also discussed. All of the benzofuran derivatives have weak anti-AChE activities compared with the reference compound, donepezil. MDPI 2010-11-29 /pmc/articles/PMC6259253/ /pubmed/21116228 http://dx.doi.org/10.3390/molecules15128593 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Zhou, Xiang Li, Miao Wang, Xiao-Bing Wang, Tao Kong, Ling-Yi Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase |
title | Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase |
title_full | Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase |
title_fullStr | Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase |
title_full_unstemmed | Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase |
title_short | Synthesis of Benzofuran Derivatives via Rearrangement and Their Inhibitory Activity on Acetylcholinesterase |
title_sort | synthesis of benzofuran derivatives via rearrangement and their inhibitory activity on acetylcholinesterase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259253/ https://www.ncbi.nlm.nih.gov/pubmed/21116228 http://dx.doi.org/10.3390/molecules15128593 |
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