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Tricyclic isoindolines by Heck cyclization
, M.E. Maier
Published in
2012
Volume: 68
   
Issue: 6
Pages: 1745 - 1749
Abstract
A series of 4-formyl esters 8a-d was prepared by Michael addition of an enamine with ethyl acrylate. A subsequent condensation with 2-bromobenzylamines 3 gave rise to cyclic enamides 9aa-dd. In a Heck cyclization reaction tricyclic isoindoles 10aa-dd were formed in good yields. © 2011 Elsevier Ltd. All rights reserved.
About the journal
JournalTetrahedron
ISSN00404020