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.issued
2019-07-12T07:51:31Z
dc.date.issued
2020-05-27T05:10:24Z
dc.date.issued
2019-05-27
dc.date.issued
2019-07-12T07:51:32Z
dc.identifier
https://hdl.handle.net/2445/137117
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.
dc.format
application/pdf
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/openAccess
dc.source
Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)
dc.subject
Compostos heterocíclics
dc.subject
Síntesi orgànica
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
