A General, Diastereoselective Synthesis of Highly Functionalized Bicyclo[<i>n</i>.3.1]alkane Systems Based on an Anionic Domino Reaction of α‐Nitrocycloalkanones

The base-promoted Michael–aldol anionic domino reactions of cyclic α-nitro ketones and α,β-unsaturated aldehydes afforded bicyclo[n.3.1]alkanone systems of seven different ring sizes (n = 3–9), normally in excellent yields. This can be considered the first general method for the synthesis of this ty...

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Detalles Bibliográficos
Autores: Rodriguez, Jean, Giorgi Poletti, Giorgio, Ruiz Serrano, Miriam, López-Alvarado Gutiérrez, María Pilar, Menéndez Ramos, José Carlos
Tipo de recurso: artículo
Fecha de publicación:2011
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/128700
Acceso en línea:https://hdl.handle.net/20.500.14352/128700
Access Level:acceso abierto
Palabra clave:547
Bicyclic compounds
Domino reactions
Michael addition
Aldol reactions
Diastereoselectivity
Química orgánica (Química)
2306.04 Química de Los Compuestos Bicíclicos
Descripción
Sumario:The base-promoted Michael–aldol anionic domino reactions of cyclic α-nitro ketones and α,β-unsaturated aldehydes afforded bicyclo[n.3.1]alkanone systems of seven different ring sizes (n = 3–9), normally in excellent yields. This can be considered the first general method for the synthesis of this type of carbocycle. Furthermore, up to four stereocentres are generated, three of which are contiguous and include a functionalized quaternary bridgehead carbon atom. The diastereoselectivity was often complete, was much higher than in les general reactions based on related domino processes, and involved the generation of a different major diastereomer due to the control of the Michael and aldol individual steps of the reaction by the nitro group