Enantioselective synthesis of lepadins A D from a phenylglycinol-derived hydroquinolone lactam

The marine alkaloids (-)-lepadins A-C and (+)-lepadin D, belonging to two diastereoisomeric series, were synthesized from an (R)-phenylglycinol-derived tricyclic lactam via a common cis-decahydroquinoline intermediate. Crucial aspects of the synthesis are the stereochemical control in the assembly o...

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Detalles Bibliográficos
Autores: Amat Tusón, Mercedes, Pinto, Alexandre, Griera Farres, Rosa, Bosch Cartes, Joan
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2015
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/108026
Acceso en línea:https://hdl.handle.net/2445/108026
Access Level:acceso abierto
Palabra clave:Alcaloides
Lactames
Compostos heterocíclics
Síntesi asimètrica
Alkaloids
Lactams
Heterocyclic compounds
Asymmetric synthesis
Descripción
Sumario:The marine alkaloids (-)-lepadins A-C and (+)-lepadin D, belonging to two diastereoisomeric series, were synthesized from an (R)-phenylglycinol-derived tricyclic lactam via a common cis-decahydroquinoline intermediate. Crucial aspects of the synthesis are the stereochemical control in the assembly of the cis-decahydroquinoline platform, in the introduction of the C2 methyl and C3 hydroxy substituents, and in the generation of the C5 stereocenter.