Publication:
Asymmetric Synthesis of Trifluoromethylated ent-Fragransin C <inf>1</inf>

dc.contributor.authorSasirome Racochoteen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorPawaret Leowanawaten_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-01-27T08:13:54Z
dc.date.available2020-01-27T08:13:54Z
dc.date.issued2019-03-31en_US
dc.description.abstract© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Asymmetric synthesis of trifluoromethylated derivative of ent-fragransin C 1 was reported. The installation of contiguous stereochemistries across the tetrahydrofuran scaffold was achieved through stereocontrolled conjugate addition, aldol reaction, and a protection-free intramolecular C-O bond formation (furan ring formation) via chemoselective generation of the benzylic carbocation.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. Vol.2019, No.12 (2019), 2212-2223en_US
dc.identifier.doi10.1002/ejoc.201801676en_US
dc.identifier.issn10990690en_US
dc.identifier.issn1434193Xen_US
dc.identifier.other2-s2.0-85060334645en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50573
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060334645&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleAsymmetric Synthesis of Trifluoromethylated ent-Fragransin C <inf>1</inf>en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060334645&origin=inwarden_US

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