Synlett 2007(5): 0741-0744  
DOI: 10.1055/s-2007-970778
LETTER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 2-Aza-1-cyano-4-hydroxyanthraquinones

Sven Claessens, Jan Jacobs, Norbert De Kimpe*
Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, 9000 Ghent, Belgium
Fax: +32(9)2646243; e-Mail: norbert.dekimpe@UGent.be;
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Publikationsverlauf

Received 28 December 2006
Publikationsdatum:
08. März 2007 (online)

Abstract

Phthalide annulation of 2-alkylpyridin-3-ones results in the formation of the unexpected 2-aza-1-cyano-4-hydroxy-anthraquinones, the cyano moiety originating from the 3-cyanophthalide. These compounds hold great potential against Epstein-Barr Virus Early Antigen (EBV-EA) activation and as antimicrobial compounds