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dc.contributor.authorAshraf M. Omaren_US
dc.contributor.authorSijia Sunen_US
dc.contributor.authorMin Jo Kimen_US
dc.contributor.authorAhmed M. Tawilaen_US
dc.contributor.authorDya Fita Dibween_US
dc.contributor.authorAmpai Phrutivorapongkulen_US
dc.contributor.authorNaoki Toyookaen_US
dc.contributor.authorSuresh Awaleen_US
dc.date.accessioned2020-10-14T08:25:35Z-
dc.date.available2020-10-14T08:25:35Z-
dc.date.issued2020-07-16en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-85086176895en_US
dc.identifier.other10.1016/j.tetlet.2020.152099en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85086176895&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70203-
dc.description.abstract© 2020 Elsevier Ltd Phytochemical investigation of Anneslea fragrans twigs resulted in the discovery of fragranol A (1), a new class of structurally challenging and sterically hindered “spiro-triflavanoid” type compound possessing an unprecedented carbon skeleton. Fragranol A (1) consists of 45 carbons having six chiral carbons, including two spiro-chiral centers. Structural elucidation of 1 was achieved by HRFABMS, 1D and 2D NMR, analysis of spatial anisotropic effects, and quantum ECD calculations. A plausible biogenetic pathway of 1 is also proposed.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFragranol A: A new class of spiro-triflavanoid hybrid with an unprecedented carbon skeleton from Anneslea fragransen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume61en_US
article.stream.affiliationsUniversity of Toyamaen_US
article.stream.affiliationsChiang Mai Universityen_US
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