Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/96647
Type: Artigo de periódico
Title: Synthesis Of Pentabromopseudilin And Other Arylpyrrole Derivatives Via Heck Arylations
Author: Schwalm C.S.
De Castro I.B.D.
Ferrari J.
De Oliveira F.L.
Aparicio R.
Correia C.R.D.
Abstract: Pentrabromopseudilin and other 2 and 3-arylpyrrole derivatives were synthesized through the Heck-Matsuda reaction involving endocyclic enecarbamates and N-protected 3-pyrrolines, respectively. The overall processes permitted an easy and efficient access to these structural motifs present in several bioactive compounds. Attempts to synthesize the compound isopentabromopseudilin led to a tribromo aryl maleimide. We hypothesize that this latter compound is the putative product arising from the unusual thermal instability of isopentabromopseudilin. © 2011 Elsevier Ltd. All rights reserved.
Editor: 
Rights: fechado
Identifier DOI: 10.1016/j.tetlet.2012.01.086
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-84857356595&partnerID=40&md5=3e9f7f4ea0d02ad128a92b6f46d317d1
Date Issue: 2012
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.