Enantioselective formal synthesis of (+)-madangamine A

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dc.contributor	Universitat de Barcelona
dc.contributor.author	Are, Celeste
dc.contributor.author	Pérez Bosch, Maria
dc.contributor.author	Bosch Cartes, Joan
dc.contributor.author	Amat Tusón, Mercedes
dc.date	2019-07-12T07:51:31Z
dc.date	2019-05-27
dc.date	2019-07-12T07:51:32Z
dc.date	info:eu-repo/date/embargoEnd/2020-05-27
dc.identifier.citation	1359-7345
dc.identifier.citation	690329
dc.identifier.uri	http://hdl.handle.net/2445/137117
dc.format	application/pdf
dc.language.iso	eng
dc.publisher	Royal Society of Chemistry
dc.relation	Versió postprint del document publicat a: https://doi.org/10.1039/c9cc03690c
dc.relation	Chemical Communications, 2019
dc.relation	https://doi.org/10.1039/c9cc03690c
dc.rights	(c) Are, Celeste et al., 2019
dc.rights	info:eu-repo/semantics/embargoedAccess
dc.subject	Alcaloides
dc.subject	Lactames
dc.subject	Compostos heterocíclics
dc.subject	Síntesi orgànica
dc.subject	Alkaloids
dc.subject	Lactams
dc.subject	Heterocyclic compounds
dc.subject	Organic synthesis
dc.title	Enantioselective formal synthesis of (+)-madangamine A
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/acceptedVersion
dc.description.abstract	An enantioselective formal synthesis of the marine alkaloid madangamine A using phenylglycinol-derived lactam 1 as the starting enantiomeric scaffold is reported. The synthesis involves the construction of the C-9 substituted diazatricyclic ABC core and the final closure of D and E rings from the polyunsaturated skipped intermediate 19.