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Iodomethyl phenyl sulfoxide: reactivity and synthetic applications

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dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorChitchanun Panyachotipunen_US
dc.contributor.authorViwat Hahnvajanawongen_US
dc.contributor.authorS. Sotheeswaranen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Peradeniyaen_US
dc.date.accessioned2018-10-12T07:40:24Z
dc.date.available2018-10-12T07:40:24Z
dc.date.issued1984-01-01en_US
dc.description.abstractLithio iodomethyl phenyl sulfoxides reacted with alkyl halides and carbonyl compounds to give adducts in good to moderate yields. Solvolysis of the carbonyl adducts led to sulfones or the ring expanded product. © 1984.en_US
dc.identifier.citationTetrahedron Letters. Vol.25, No.17 (1984), 1825-1828en_US
dc.identifier.doi10.1016/S0040-4039(01)90051-6en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-48749133877en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/30586
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=48749133877&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleIodomethyl phenyl sulfoxide: reactivity and synthetic applicationsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=48749133877&origin=inwarden_US

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