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Samarium(II) iodide-mediated deoxygenative debromination of α-bromo-β-hydroxy (acetoxy) phenyl sulfones: Synthesis of α,β-unsaturated sulfones

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dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorSuwatchai Jarussophonen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorYupa Chaiyasuten_US
dc.contributor.authorSaengvimon U-Theten_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T02:57:07Z
dc.date.available2018-07-24T02:57:07Z
dc.date.issued2002-03-18en_US
dc.description.abstractDeoxygenative debromination of α-bromo-β-hydroxy (acetoxy) phenyl sulfones with samarium(II) iodide led to substituted α,β-unsaturated sulfones in good to excellent yields. The E-isomer is the major product. A possible mechanism via an α-sulfonyl radical pathway is proposed. © 2002 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.43, No.12 (2002), 2285-2288en_US
dc.identifier.doi10.1016/S0040-4039(02)00224-1en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0037128515en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/20073
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037128515&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleSamarium(II) iodide-mediated deoxygenative debromination of α-bromo-β-hydroxy (acetoxy) phenyl sulfones: Synthesis of α,β-unsaturated sulfonesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037128515&origin=inwarden_US

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