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Silver-mediated decarboxylative fluorination of paraconic acids: A direct entry to β-fluorinated γ-butyrolactones

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dc.contributor.authorSupasorn Phae-Noken_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:56:57Z
dc.date.available2018-11-23T09:56:57Z
dc.date.issued2015-05-01en_US
dc.description.abstract© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. The silver(I)-mediated decarboxylative fluorination of paraconic acids using Selectfluor<sup>®</sup> as a fluorine source is reported. Readily available paraconic acids undergo decarboxylative fluorination with Selectfluor<sup>®</sup> mediated by AgNO<inf>3</inf> to give the corresponding β-fluorinated γ-butyrolactones in moderate to good yields. This approach serves as a direct and site-selective strategy for the introduction of a fluorine atom at the β position of γ-butyrolactone cores. The fluorinated products are synthetically useful scaffolds for organic synthesis.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. Vol.2015, No.13 (2015), 2879-2888en_US
dc.identifier.doi10.1002/ejoc.201500023en_US
dc.identifier.issn10990690en_US
dc.identifier.issn1434193Xen_US
dc.identifier.other2-s2.0-84928036476en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/35750
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84928036476&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleSilver-mediated decarboxylative fluorination of paraconic acids: A direct entry to β-fluorinated γ-butyrolactonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84928036476&origin=inwarden_US

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