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Synthesis of alkylated indolizidine alkaloids via Pummerer mediated cyclization: synthesis of (±)-indolizidine 167B, (±)-5-butylindolizidine and (±)-monomorine I

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dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorPhachanee Seehasombaten_US
dc.contributor.authorThaworn Jaipetchen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-12T02:19:44Z
dc.date.available2018-07-12T02:19:44Z
dc.date.issued2008-02-18en_US
dc.description.abstractThe syntheses of indolizidine alkaloids, i.e., (±)-coniceine, (±)-indolizidine 167B, (±)-5-butylindolizidine and (±)-monomorine I via Pummerer cyclization are described. The key step is the transformation of lactam sulfoxide to bicyclic lactam via the Pummerer cyclization. © 2007 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron. Vol.64, No.8 (2008), 1663-1670en_US
dc.identifier.doi10.1016/j.tet.2007.12.013en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-38349057328en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/18969
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38349057328&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleSynthesis of alkylated indolizidine alkaloids via Pummerer mediated cyclization: synthesis of (±)-indolizidine 167B, (±)-5-butylindolizidine and (±)-monomorine Ien_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38349057328&origin=inwarden_US

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