AN EASY ENTRY TO ISOQUINOLINE ALKALOIDS BY AZA-WITTIG ELECTROCYCLIC RING-CLOSURE

dc.creatorRODRIGUES, JAR
dc.creatorLEIVA, GC
dc.creatorDESOUSA, JDF
dc.date1995
dc.date37257
dc.date2014-12-16T11:36:59Z
dc.date2015-11-26T16:26:02Z
dc.date2014-12-16T11:36:59Z
dc.date2015-11-26T16:26:02Z
dc.date.accessioned2018-03-28T23:06:47Z
dc.date.available2018-03-28T23:06:47Z
dc.identifierTetrahedron Letters. Pergamon-elsevier Science Ltd, v. 36, n. 1, n. 59, n. 62, 1995.
dc.identifier0040-4039
dc.identifierWOS:A1995PZ49000012
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/54356
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/54356
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/54356
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1268772
dc.descriptionThe reaction of phenethyliminophosphorane with arylketenes gave 1-benzyl-3.4-dihydroisoquinolines in good yields. An aza-Wittig type reaction of vinyliminophosphorane with p-toluenesulfonylisocyanate furnished 1-aminoisoquinoline 6 in high yield.
dc.description36
dc.description1
dc.description59
dc.description62
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationTetrahedron Letters
dc.relationTetrahedron Lett.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectAZA-WITTIG REACTION
dc.subjectISOQUINOLINES
dc.subjectIMINOPHOSPHORANES
dc.subjectKETENES
dc.subjectDerivatives
dc.titleAN EASY ENTRY TO ISOQUINOLINE ALKALOIDS BY AZA-WITTIG ELECTROCYCLIC RING-CLOSURE
dc.typeArtículos de revistas


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