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PhI(OAc)<inf>2</inf>/KI mediated 1,2-acetoxysulfenylation of alkenes: Facile synthesis of β-acetoxysulfides

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dc.contributor.authorCharoensak Muangkaewen_US
dc.contributor.authorPraewpan Katrunen_US
dc.contributor.authorPatcharaphon Kanchanarugeeen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorThaworn Jaipetchen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-19T04:35:04Z
dc.date.available2018-10-19T04:35:04Z
dc.date.issued2013-10-21en_US
dc.description.abstractA convenient method for 1,2-acetoxysulfenylation of alkenes using disulfide promoted by (diacetoxyiodo)benzene (PhI(OAc)2, DIB)/KI was developed. The reaction is highly regioselective for styrene derivatives while aliphatic alkenes lead to a mixture of two regioisomers. © 2013 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron. Vol.69, No.42 (2013), 8847-8856en_US
dc.identifier.doi10.1016/j.tet.2013.08.018en_US
dc.identifier.issn14645416en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-84883487957en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/31187
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883487957&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titlePhI(OAc)<inf>2</inf>/KI mediated 1,2-acetoxysulfenylation of alkenes: Facile synthesis of β-acetoxysulfidesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883487957&origin=inwarden_US

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