Download PDF
Synlett 1998; 1998(1): 87-89
DOI: 10.1055/s-1998-1571
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

New Synthesis of Carbazoles from Novel exo-2-Oxazolidinone Dienes

Ashis B. Mandal* , Francisco Delgado, Joaquín Tamariz
  • *Department of Organic Chemistry, Escuela Nacional de Ciencias Biológicas, I.P.N. Prol. Carpio y Plan de Ayala, 11340 México, D.F.; Fax +5 25-3 96-35 03; E-mail: fdelgado@woodward.encb.ipn.mx
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

A new synthesis of carbazoles, via regioselective Diels-Alder reaction of novel exo-2-oxazolidinone dienes 1, is described. Cyclization with palladium acetate of the intermediate diaryl amines, obtained by a one-pot three-step procedure from the cycloadducts, yielded the desired substituted carbazoles.

carbazoles - exo-2-oxazolidinone dienes - Diels-Alder - palladium

      >