Synthesis 2014; 46(11): 1469-1474
DOI: 10.1055/s-0033-1338609
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Pyridoacridines through Anionic Cascade Ring Closure

Authors

  • Ida Nymann Petersen

    Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark   Fax: +4535336040   Email: jesper.kristensen@sund.ku.dk
  • Jesper Langgaard Kristensen*

    Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark   Fax: +4535336040   Email: jesper.kristensen@sund.ku.dk
Further Information

Publication History

Received: 28 January 2014

Accepted after revision: 21 February 2014

Publication Date:
21 March 2014 (online)


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Abstract

A new synthesis of 13-deazaascididemin (AK-37) based on a recently developed anionic cascade ring closure is presented. Although the isolated yields are modest, the approach provides ready access to new substituted derivatives of 13-deazaascididemin.

Supporting Information