Synthesis and cytotoxic activity of 7-oxo-7 H-dibenz [f, ij] isoquinoline and 7-oxo-7 H-benzo [e] perimidine derivatives
X Bu, LW Deady, GJ Finlay, BC Baguley…
Index: Bu; Deady; Finlay; Baguley; Denny Journal of Medicinal Chemistry, 2001 , vol. 44, # 12 p. 2004 - 2014
Full Text: HTML
Citation Number: 77
Abstract
A series of 7-oxo-7 H-dibenz [f, ij] isoquinoline and 7-oxo-7 H-benzo [e] perimidines bearing cationic side chains were prepared from aminoanthraquinones. The perimidines were prepared from 1-aminoanthraquinone by initial condensation with urea or dimethylacetamide. A series of 2-, 4-, 8-, and 11-carboxy derivatives of the dibenzisoquinolines were prepared from aminoanthraquinonecarboxylic acids. The ...
Related Articles:
Reactions of 1, 5-dichloroanthraquinone with nucleophiles
[Ruediger, Edward H.; Kaldas, Magdy L.; Ghandi. Sham S.; Fedryna, Cristi; Gibson, Martin S. Journal of Organic Chemistry, 1980 , vol. 45, # 10 p. 1974 - 1978]
A facile method for preparing substituted 1-aminoanthraquinones
[Synthetic Communications, , vol. 23, # 22 p. 3211 - 3222]
[Journal of Medicinal Chemistry, , vol. 44, # 12 p. 2004 - 2014]
Synthesis of Naphth (1, 2, 3-cd) indol-6 (2H)-one Derivatives and Their Fluorescence Properties.
[Bulletin of the Chemical Society of Japan, , vol. 64, # 11 p. 3417 - 3421]
Synthesis of Naphth (1, 2, 3-cd) indol-6 (2H)-one Derivatives and Their Fluorescence Properties.
[Bulletin of the Chemical Society of Japan, , vol. 64, # 11 p. 3417 - 3421]