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6,7,14,15-Tetrahydro-15aH-azocino[1,2-a:6,5-b']diindole.Synthesis of a novel pentacyclic ring system

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dc.contributor.authorKittisak Sriphaen
dc.contributor.authorZlotos, Darius P.en
dc.contributor.authorBuller, Stefanen
dc.contributor.authorMohr, Klausen
dc.contributor.otherMahidol University. Faculty of Pharmacy. Department of Pharmaceutical Chemistry.
dc.contributor.otherUniversity of Wurzburg. Pharmaceutical Institute.
dc.date.accessioned2010-08-09T03:40:20Zen
dc.date.accessioned2011-07-08T07:36:18Z
dc.date.accessioned2021-05-07T07:35:18Z
dc.date.available2010-08-09T03:40:20Zen
dc.date.available2011-07-08T07:36:18Z
dc.date.available2021-05-07T07:35:18Z
dc.date.created2010-08-09T03:40:20Zen
dc.date.issued2003en
dc.description.abstractIn search of new lead structures for potent allosteric enhancers of antagonist binding to muscarinic M2 receptors, a novel heterocyclic ring system, 6,7,14,15-tetrahydro-15aH-azocino[1,2-a:6,5-b′]diindole, has been synthesized. The new ring skeleton was obtained from indol-2-yl-acetic acid in three steps.
dc.format.extent140273 bytesen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationTetrahedron Letters. Vol.44, No.38 (2003),7183-6.
dc.identifier.doi10.1016/S0040-4039(03)01796-9
dc.identifier.issn0040-4039en
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/62090
dc.language.isoengen
dc.rightsMahidol Universityen
dc.rights.holderPergamon (available from ScienceDirect)
dc.sourceTetrahedron Letters
dc.sourceScienceDirect
dc.subject6,7,14,15-tetrahydro-15aH-azocino[1,2-a:6,5-a']diindoleen
dc.subjectnovel pentacyclic ring systemen
dc.subjectStrychnos alkaloid caracurine Ven
dc.subjectdimerization of 2-(indol-2-yl)-ethyl tosylateen
dc.title6,7,14,15-Tetrahydro-15aH-azocino[1,2-a:6,5-b']diindole.Synthesis of a novel pentacyclic ring systemen
dc.typeOriginal Articleen
dcterms.dateAccepted2003-07-24
dspace.entity.typePublication
mods.location.urlhttps://www.sciencedirect.com/science/article/abs/pii/S0040403903017969

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