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Please use this identifier to cite or link to this item: http://dspace.utalca.cl/handle/1950/3337

Title: An efficient synthesis of hexahydro oxaisoindolo[2,1-a]quinoline derivatives via the Diels-Alder reactions
Authors: Kouznetsov, V.V.
Zubkov, F. I.
Cruz, U.M.
Voskressensky, L.G.
Mendez, L.Y.V.
Astudillo, L.
Stashenko, E.E.
Issue Date: Jan-2004
Publisher: Bentham Science Publisher Ltd.
Citation: Letters in Organic Chemistry 1 (1): 37-39
Abstract: he straight forward synthesis of new carboxylic acids with hexahydro-oxaisoindolo[2.1-a]quinoline core from the 2,4-disustituted 1,2,3,4-tetrallydroquinolines bearing a furan fragment via the intramolecular Diels-Alder reaction has been proposed. It was demonstrated that synthesis of key precursors can be realized with excellent level of diastereoselectivity either by imino-Diels-Alder reaction or multi-component condensation approach.
Description: Kouznetsov, V.V. (reprint author), Univ Talca, Inst Quim Recursos Nat, Lab Sintesis Organ, Casilla 747, Talca, Chile.
URI: http://dspace.utalca.cl/handle/1950/3337
ISSN: 1570-1786
Appears in Collections:Artículos en publicaciones ISI - Universidad de Talca

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