Tetrahedron Letters p. 4309 - 4312 (1989)
Update date:2022-08-05
Topics: Regioselectivity Lewis acid Column chromatography Yield NMR spectroscopy Catalyst Synthetic route HPLC (high-performance liquid chromatography) Diels-Alder Reaction Stereoselectivity Cycloaddition Tautomerization Dienophile Diene Functionalised Heterocycle Electron-withdrawing group Electron-donating group Retro-Diels-Alder
Imbroisi, Dennis de Oliveira
Simpkins, Nigel S.
A new substituted 5,6-dihydro-2(1H)-pyridinone participates in highly efficient Diels-Alder reactions to give functionalised cis-hydroisoquinolines suitable for natural product synthesis.
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