SnO2 nanoparticles mediated nontraditional synthesis of biologically active 9-chloro-6,13-dihydro-7-phenyl-5H-indolo [3,2-c]-acridine derivatives
HeLa
Acridine derivatives
Acridine
Methylene
Vero cell
DOI:
10.1007/s00044-010-9381-7
Publication Date:
2010-06-29T01:57:04Z
AUTHORS (2)
ABSTRACT
An efficient, practical, and eco-friendly method of preparation of 9-chloro-6,13-dihydro-7-phenyl-5H-indolo[3,2-c]-acridines (3a–c) is reported by Friedlander condensation of 2-amino-5-chlorobenzophenone 1 and active methylene compound 3,4-dihydro-2H-carbazol-1(9H)-ones (2a–c) in the presence of SnO2 nanoparticles under microwave irradiation. Indoloacridines, 3a–c, were screened for their in vitro hemolytic activity, on human erythrocytes and cytotoxicity, on HeLa and Vero cells.
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