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Further developments in the synthesis of lamellarin alkaloids via direct metal-halogen exchange

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dc.contributor.authorPoonsakdi Ploypradithen_US
dc.contributor.authorWiyada Jinagluengen_US
dc.contributor.authorChitkavee Pavaroen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:20:50Z
dc.date.available2018-07-24T03:20:50Z
dc.date.issued2003-02-10en_US
dc.description.abstractDirect metal-halogen exchange of 2-bromopyrrole carbonate derivatives with tert-butyllithium followed by the intramolecular lactonization of the resulting 2-pyrrole anion onto the carbonate provided the corresponding lamellarins in moderate to good yield. The lamellarin framework could be obtained from the direct metal-halogen exchange strategy in a 26-33% overall yield over 5-6 steps. © 2003 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.44, No.7 (2003), 1363-1366en_US
dc.identifier.doi10.1016/S0040-4039(02)02887-3en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-0037429073en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/20762
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037429073&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFurther developments in the synthesis of lamellarin alkaloids via direct metal-halogen exchangeen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0037429073&origin=inwarden_US

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