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dc.contributor.authorRatchanok Pingaewen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.date.accessioned2018-08-24T01:45:55Z-
dc.date.available2018-08-24T01:45:55Z-
dc.date.issued2007-09-17en_US
dc.identifier.citationSynlett. No.15 (2007), 2363-2366en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-34948839846en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34948839846&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/24337-
dc.description.abstractThe oxidative biaryl coupling of various N-substituted 1- benzyltetrahydroisoquinolines to the corresponding aporphines by the hypervalent iodine reagent was studied. The study sheds light on the unifying mechanism of the reaction illustrating the requirement of the p-p coupling via the six-membered transition state as the initial step. The finding was applied to the synthesis of some pentasubstituted aporphine alkaloids. © Georg Thieme Verlag Stuttgart.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34948839846&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleApplication of the hypervalent iodine reagent to the synthesis of some pentasubstituted aporphine alkaloidsen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1055/s-2007-985596en_US
Appears in Collections:Scopus 2006-2010

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