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α,α-Difluoro-α-phenylsulfanyl-α- trimethylsilylmethane as "cF<inf>2</inf><sup>-</sup>" synthetic building block for the preparation of gem-difluoromethylenated cyclopentanols

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dc.contributor.authorKrisana Peewasanen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-11T04:38:34Z
dc.date.available2018-06-11T04:38:34Z
dc.date.issued2012-03-01en_US
dc.description.abstractA general strategy for the preparation of gem-difluoromethylenated cyclopentanols has been demonstrated; it involves sequential fluoride-catalyzed nucleophilic addition of α,α-difluoro-α-phenylsulfanyl- α-trimethylsilylmethane (PhSCF 2 SiMe 3 ; 1) to homoallyl ketones followed by intramolecular radical cyclization. © 2011 Elsevier B.V. All rights reserved.en_US
dc.identifier.citationJournal of Fluorine Chemistry. Vol.135, (2012), 367-372en_US
dc.identifier.doi10.1016/j.jfluchem.2011.10.009en_US
dc.identifier.issn00221139en_US
dc.identifier.other2-s2.0-84857368913en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/13780
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84857368913&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectEnvironmental Scienceen_US
dc.titleα,α-Difluoro-α-phenylsulfanyl-α- trimethylsilylmethane as "cF<inf>2</inf><sup>-</sup>" synthetic building block for the preparation of gem-difluoromethylenated cyclopentanolsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84857368913&origin=inwarden_US

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