A general approach to N-heterocyclic scaffolds using domino Heck-aza-Michael reactions


Autoria(s): Priebbenow, Daniel L.; Stewart, Scott G.; Pfeffer, Frederick M.
Data(s)

01/01/2011

Resumo

Palladium-catalyzed domino Heck–aza-Michael reactions for the synthesis of a series of C1-substituted tetrahydro-β-carbolines, tetrahydroisoquinolines and isoindolines are described. The domino process involves the initial intermolecular Heck reaction of an aryl bromide with an electron deficient alkene, followed by an intramolecular aza-Michael reaction to form the new N-heterocycle in high yield.

Identificador

http://hdl.handle.net/10536/DRO/DU:30040415

Idioma(s)

eng

Publicador

Royal Society of Chemistry

Relação

http://dro.deakin.edu.au/eserv/DU:30040415/priebbenow-ageneralapproach-2011.pdf

http://dx.doi.org/10.1039/c0ob00835d

Direitos

2011, The Royal Society of Chemistry

Tipo

Journal Article