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Efficient Formal Total Synthesis of the Erythrina Alkaloid (+)-Erysotramidine, Using a Domino Process

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dc.bibliographiccitation.firstpage5230
dc.bibliographiccitation.issue22
dc.bibliographiccitation.journalOrganic Letters
dc.bibliographiccitation.lastpage5233
dc.bibliographiccitation.volume11
dc.contributor.authorTietze, Lutz Friedjan
dc.contributor.authorToelle, Nina
dc.contributor.authorKratzert, Daniel
dc.contributor.authorStalke, Dietmar
dc.date.accessioned2018-11-07T11:21:59Z
dc.date.available2018-11-07T11:21:59Z
dc.date.issued2009
dc.description.abstractA domino process consisting of an amidation, spirocyclization, and formation of an iminium Ion and electrophilic aromatic substitution of a phenylethylamine and a ketoester leads to the spirocyclic skeleton of (+)-erysotramidine, which can be further transformed into the natural alkaloid.
dc.description.sponsorshipDeutsche Forschungsgemeinschaft; Fonds der Chemischen Industrie
dc.identifier.doi10.1021/ol901980u
dc.identifier.isi000271583000035
dc.identifier.pmid19860384
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/55902
dc.notes.statuszu prüfen
dc.notes.submitterNajko
dc.publisherAmer Chemical Soc
dc.relation.issn1523-7060
dc.titleEfficient Formal Total Synthesis of the Erythrina Alkaloid (+)-Erysotramidine, Using a Domino Process
dc.typejournal_article
dc.type.internalPublicationyes
dc.type.peerReviewedyes
dc.type.statuspublished
dspace.entity.typePublication

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