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

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
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Publikationsverlauf

Received: 28. Januar 2014

Accepted after revision: 21. Februar 2014

Publikationsdatum:
21. März 2014 (online)


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

 
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