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Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp.
A new piperidone alkaloid, dysidone A (1), was isolated from the marine sponge Dysidea sp. The structure of 1 was elucidated by the method of spectroscopic analysis. Compound 1 represented the first example of piperidone alkaloid isolated from the sponge of the genus Dysidea with the exocyclic doubl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557106/ https://www.ncbi.nlm.nih.gov/pubmed/37809021 http://dx.doi.org/10.1039/d3ra06115a |
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author | Lei, Yu Li, Boao Liao, Xiaojian Xing, Xiwen Feng, Pengju Zhao, Bingxin Xu, Shihai |
author_facet | Lei, Yu Li, Boao Liao, Xiaojian Xing, Xiwen Feng, Pengju Zhao, Bingxin Xu, Shihai |
author_sort | Lei, Yu |
collection | PubMed |
description | A new piperidone alkaloid, dysidone A (1), was isolated from the marine sponge Dysidea sp. The structure of 1 was elucidated by the method of spectroscopic analysis. Compound 1 represented the first example of piperidone alkaloid isolated from the sponge of the genus Dysidea with the exocyclic double bond. Furthermore, the total synthesis of 1 was also carried out, which was started with piperidine proceeding a PIDA/I(2)-mediated α and β-C (sp(3)) –H bond dual oxygenation to achieve a 5-steps synthesis in a total yield of 10.6%. In addition, the anti-inflammatory activities of 1 and its derivative dysidone B (1d) were evaluated, which suggested that 1 showed weak anti-inflammatory activity. |
format | Online Article Text |
id | pubmed-10557106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-105571062023-10-07 Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. Lei, Yu Li, Boao Liao, Xiaojian Xing, Xiwen Feng, Pengju Zhao, Bingxin Xu, Shihai RSC Adv Chemistry A new piperidone alkaloid, dysidone A (1), was isolated from the marine sponge Dysidea sp. The structure of 1 was elucidated by the method of spectroscopic analysis. Compound 1 represented the first example of piperidone alkaloid isolated from the sponge of the genus Dysidea with the exocyclic double bond. Furthermore, the total synthesis of 1 was also carried out, which was started with piperidine proceeding a PIDA/I(2)-mediated α and β-C (sp(3)) –H bond dual oxygenation to achieve a 5-steps synthesis in a total yield of 10.6%. In addition, the anti-inflammatory activities of 1 and its derivative dysidone B (1d) were evaluated, which suggested that 1 showed weak anti-inflammatory activity. The Royal Society of Chemistry 2023-10-06 /pmc/articles/PMC10557106/ /pubmed/37809021 http://dx.doi.org/10.1039/d3ra06115a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Lei, Yu Li, Boao Liao, Xiaojian Xing, Xiwen Feng, Pengju Zhao, Bingxin Xu, Shihai Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. |
title | Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. |
title_full | Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. |
title_fullStr | Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. |
title_full_unstemmed | Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. |
title_short | Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp. |
title_sort | isolation and total synthesis of dysidone a: a new piperidone alkaloid from the marine sponge dysidea sp. |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557106/ https://www.ncbi.nlm.nih.gov/pubmed/37809021 http://dx.doi.org/10.1039/d3ra06115a |
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