An efficient synthesis of new C-2 aryl substituted quinolines based on three component imino Diels-Alder reaction

dc.creator	Kouznetsov, V.V.
dc.creator	Bohorquez, A.R.R.
dc.creator	Astudillo, L.
dc.creator	Medina, R.F.
dc.date	2008-03-10T14:51:57Z
dc.date	2008-03-10T14:51:57Z
dc.date	2006
dc.date.accessioned	2017-03-07T14:45:23Z
dc.date.available	2017-03-07T14:45:23Z
dc.identifier	Molecular Diversity 10 (1):29-37
dc.identifier	1381-1991
dc.identifier	http://dspace.utalca.cl/handle/1950/4614
dc.identifier.uri	http://repositorioslatinoamericanos.uchile.cl/handle/2250/372289
dc.description	Astudillo, L. Instituto de Química de Recursos Naturales, Universidad de Talca, Casilla: 747, Talca, Chile.
dc.description	New effective approach to the synthesis of a wide variety of C-2 nitro or aminophenyl substituted quinolines was reported using diverse intermediate 4-(2-oxopyrrolinidyl-1)-tetrahydroquinolines that were prepared by a three component imino Diels-Alder reaction was reported. The key aromatisation process occurs cleanly with the loss of the 2-oxopyrrolinidyl-1 fragment.
dc.format	2974 bytes
dc.format	text/html
dc.language	en
dc.publisher	Springer Netherlands
dc.subject	C-2 substituted quinolines; three component imino Diels-Alder reaction
dc.title	An efficient synthesis of new C-2 aryl substituted quinolines based on three component imino Diels-Alder reaction
dc.type	Artículos de revistas