Synlett 2012; 23(5): 791-795
DOI: 10.1055/s-0031-1290164
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© Georg Thieme Verlag Stuttgart · New York

Microwave-Promoted Michael Addition of Azaheterocycles to α,β-Unsaturat­ed Esters and Acid under Solvent-Free Conditions

Authors

  • Lilian Dubois

    Université Paris Descartes, Sorbonne Paris Cité, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 Rue des Saints-Pères, 75270 Paris Cedex 06, France, Fax: +33(1)4286218387   Email: isabelle.mccort@parisdescartes.fr
  • Francine C. Acher

    Université Paris Descartes, Sorbonne Paris Cité, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 Rue des Saints-Pères, 75270 Paris Cedex 06, France, Fax: +33(1)4286218387   Email: isabelle.mccort@parisdescartes.fr
  • Isabelle McCort-Tranchepain*

    Université Paris Descartes, Sorbonne Paris Cité, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 Rue des Saints-Pères, 75270 Paris Cedex 06, France, Fax: +33(1)4286218387   Email: isabelle.mccort@parisdescartes.fr
Further Information

Publication History

Received: 09 November 2011

Accepted after revision: 04 January 2012

Publication Date:
09 February 2012 (online)


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Abstract

Regioselective Michael addition of N-9 adenine to ethyl acrylate under microwave activation in solid-liquid solvent-free phase-transfer catalysis using TBAB as catalyst and DABCO as base was extended to tert-butyl acrylate and acrylic acid. Under these conditions and in the presence of a catalytic amount of KOH, first Michael addition of indole and indolylmaleimide to acrylates is also reported.

Supporting Information