Publication:
Stereoselective nucleophilic addition of PhSCF<inf>2</inf>SiMe<inf>3</inf> to chiral cyclic nitrones: Asymmetric synthesis of gem-difluoromethylenated polyhydroxypyrrolizidines and -indolizidines

dc.contributor.authorKorkit Korvorapunen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:58:23Z
dc.date.available2018-11-23T09:58:23Z
dc.date.issued2015-01-01en_US
dc.description.abstract© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Fluoride-catalyzed nucleophilic addition of a difluoro(phenylsulfanyl)methyl group ("PhSCF2") generated from PhSCF2SiMe3 to nitrones was accomplished in satisfactory yields. High diastereoselectivities were observed with chiral polyoxygenated cyclic nitrones to provide the corresponding adducts, which were further manipulated to afford gem-difluoromethylenated polyhydroxypyrrolizidines and -indolizidines.en_US
dc.identifier.citationChemistry - An Asian Journal. Vol.10, No.4 (2015), 948-968en_US
dc.identifier.doi10.1002/asia.201403023en_US
dc.identifier.issn1861471Xen_US
dc.identifier.issn18614728en_US
dc.identifier.other2-s2.0-84925590476en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/35763
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84925590476&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleStereoselective nucleophilic addition of PhSCF<inf>2</inf>SiMe<inf>3</inf> to chiral cyclic nitrones: Asymmetric synthesis of gem-difluoromethylenated polyhydroxypyrrolizidines and -indolizidinesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84925590476&origin=inwarden_US

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