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dc.contributor.authorNopporn Thasanaen_US
dc.contributor.authorBen Bjerke-Krollen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.otherChulabhorn Graduate Instituteen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.date.accessioned2018-07-12T02:23:19Z-
dc.date.available2018-07-12T02:23:19Z-
dc.date.issued2008-03-03en_US
dc.identifier.citationSynlett. No.4 (2008), 505-508en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-40949157622en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40949157622&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/19088-
dc.description.abstractA facile one-pot synthesis of 2,3-dioxopyrrolo[2,1-a]isoquinolines is reported involving the ring formation of aryl pyruvate derivatives with 3,4-dihydroisoquinolines under basic conditions and utilizing the Reformatsky reaction. Using microwave irradiation, the required compounds were obtained in moderate to good yields. © Georg Thieme Verlag Stuttgart.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40949157622&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleA facile synthesis of telisatin A via microwave-promoted annulation and reformatsky reactionen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1055/s-2008-1042764en_US
Appears in Collections:Scopus 2006-2010

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