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Structural modification of oridonin: Via DAST induced rearrangement

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dc.contributor.authorDong Dong Luoen_US
dc.contributor.authorKai Pengen_US
dc.contributor.authorJia Yu Yangen_US
dc.contributor.authorPawinee Piyachaturawaten_US
dc.contributor.authorWitchuda Saengsawangen_US
dc.contributor.authorLei Aoen_US
dc.contributor.authorWan Zhou Zhaoen_US
dc.contributor.authorYu Tangen_US
dc.contributor.authorSheng Biao Wanen_US
dc.contributor.otherOcean University of Chinaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNanjing OGpharma Co. Ltd.en_US
dc.date.accessioned2019-08-23T10:46:43Z
dc.date.available2019-08-23T10:46:43Z
dc.date.issued2018-01-01en_US
dc.description.abstract© 2018 The Royal Society of 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.en_US
dc.identifier.citationRSC Advances. Vol.8, No.52 (2018), 29548-29554en_US
dc.identifier.doi10.1039/c8ra05728aen_US
dc.identifier.issn20462069en_US
dc.identifier.other2-s2.0-85052630066en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45454
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052630066&origin=inwarden_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.titleStructural modification of oridonin: Via DAST induced rearrangementen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85052630066&origin=inwarden_US

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