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α-sulfonyl radical initiated intramolecular tandem radical cyclization: Stereochemistries of a pair of doubly cyclized products

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dc.contributor.authorLindsay T. Byrneen_US
dc.contributor.authorManat Phomakotren_US
dc.contributor.authorChompoonut Poolsanongen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorBrian W. Skeltonen_US
dc.contributor.authorAllan H. Whiteen_US
dc.contributor.otherUniversity of Western Australiaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:22:08Z
dc.date.available2018-07-24T03:22:08Z
dc.date.issued2003-08-12en_US
dc.description.abstractRoom-temperature single-crystal X-ray structure determinations are recorded for trans-1,2,3,3a,9,9a-Hexahydro-cyclopenta[b]-1-benzothiapyran-4, 4-dioxide and its 3a-methyl analogue, minor products of the α-sulfonyl radical-initiated intramolecular tandem radical cyclization of H2C=CH(CH2)CRBrSO2Ph (R = H, CH3), confirming the assigned structures and rigorously establishing the trans relationship at the ring junctions.en_US
dc.identifier.citationAustralian Journal of Chemistry. Vol.56, No.7 (2003), 715-717en_US
dc.identifier.doi10.1071/CH02134en_US
dc.identifier.issn00049425en_US
dc.identifier.other2-s2.0-0042093780en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/20811
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0042093780&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleα-sulfonyl radical initiated intramolecular tandem radical cyclization: Stereochemistries of a pair of doubly cyclized productsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0042093780&origin=inwarden_US

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