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
› Author Affiliations
Further Information

Publication History

Received: 28 January 2014

Accepted after revision: 21 February 2014

Publication Date:
21 March 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