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Structural modification of oridonin via DAST induced rearrangement
A simple and efficient protocol was developed for the syntheses of oridonin analogues, i.e. 6,20-epoxy ent-kaurane diterpenoid analogues from oridonin via diethylaminosulfur trifluoride (DAST) promoted rearrangement, most of which exhibited superior anticancer activities compared with their precurso...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085272/ https://www.ncbi.nlm.nih.gov/pubmed/35547324 http://dx.doi.org/10.1039/c8ra05728a |
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author | Luo, Dong-Dong Peng, Kai Yang, Jia-Yu Piyachaturawat, Pawinee Saengsawang, Witchuda Ao, Lei Zhao, Wan-Zhou Tang, Yu Wan, Sheng-Biao |
author_facet | Luo, Dong-Dong Peng, Kai Yang, Jia-Yu Piyachaturawat, Pawinee Saengsawang, Witchuda Ao, Lei Zhao, Wan-Zhou Tang, Yu Wan, Sheng-Biao |
author_sort | Luo, Dong-Dong |
collection | PubMed |
description | A simple and efficient protocol was developed for the syntheses of oridonin analogues, i.e. 6,20-epoxy ent-kaurane diterpenoid analogues from oridonin via diethylaminosulfur trifluoride (DAST) promoted rearrangement, most of which exhibited superior anticancer activities compared with their precursor. |
format | Online Article Text |
id | pubmed-9085272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90852722022-05-10 Structural modification of oridonin via DAST induced rearrangement Luo, Dong-Dong Peng, Kai Yang, Jia-Yu Piyachaturawat, Pawinee Saengsawang, Witchuda Ao, Lei Zhao, Wan-Zhou Tang, Yu Wan, Sheng-Biao RSC Adv Chemistry A simple and efficient protocol was developed for the syntheses of oridonin analogues, i.e. 6,20-epoxy ent-kaurane diterpenoid analogues from oridonin via diethylaminosulfur trifluoride (DAST) promoted rearrangement, most of which exhibited superior anticancer activities compared with their precursor. The Royal Society of Chemistry 2018-08-20 /pmc/articles/PMC9085272/ /pubmed/35547324 http://dx.doi.org/10.1039/c8ra05728a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Luo, Dong-Dong Peng, Kai Yang, Jia-Yu Piyachaturawat, Pawinee Saengsawang, Witchuda Ao, Lei Zhao, Wan-Zhou Tang, Yu Wan, Sheng-Biao Structural modification of oridonin via DAST induced rearrangement |
title | Structural modification of oridonin via DAST induced rearrangement |
title_full | Structural modification of oridonin via DAST induced rearrangement |
title_fullStr | Structural modification of oridonin via DAST induced rearrangement |
title_full_unstemmed | Structural modification of oridonin via DAST induced rearrangement |
title_short | Structural modification of oridonin via DAST induced rearrangement |
title_sort | structural modification of oridonin via dast induced rearrangement |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085272/ https://www.ncbi.nlm.nih.gov/pubmed/35547324 http://dx.doi.org/10.1039/c8ra05728a |
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