Publication:
Synthesis of Difluoromethyl Ketones from Weinreb Amides, and Tandem Addition/Cyclization of o-Alkynylaryl Weinreb Amides

dc.contributor.authorJongkonporn Phetcharawetchen_US
dc.contributor.authorNolan M. Betterleyen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-12-21T07:08:02Z
dc.date.accessioned2019-03-14T08:03:11Z
dc.date.available2018-12-21T07:08:02Z
dc.date.available2019-03-14T08:03:11Z
dc.date.issued2017-12-15en_US
dc.description.abstract© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim [Difluoro(phenylsulfanyl)methyl]trimethylsilane (PhSCF2SiMe3) underwent a fluoride-induced nucleophilic addition to the carbonyl group of Weinreb amides to provide the corresponding difluoro(phenylsulfanyl)methyl ketones. These were converted into difluoromethyl ketones through selective reductive cleavage of the phenylsulfanyl group. The reaction of o-alkynyl Weinreb amides derived from benzoic acid derivatives resulted in the formation of cyclized products through a 5-exo-dig cyclization.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. Vol.2017, No.46 (2017), 6840-6850en_US
dc.identifier.doi10.1002/ejoc.201701322en_US
dc.identifier.issn10990690en_US
dc.identifier.issn1434193Xen_US
dc.identifier.other2-s2.0-85038082745en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/42163
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85038082745&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleSynthesis of Difluoromethyl Ketones from Weinreb Amides, and Tandem Addition/Cyclization of o-Alkynylaryl Weinreb Amidesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85038082745&origin=inwarden_US

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