Abstract
The purpose of this study was to synthesize (E)-2-benzylidene-7-chloro-9-phenyl-3,4-dihydroacridin-1(2H)-ones and investigate their larvicidal potential against Anopheles stephensi and Hippobosca maculata. Synthetic acridines are used in many commercial applications. The results obtained from FTIR, 1H and 13C NMR, and ESI–MS spectra confirm the synthesis of (E)-2-benzylidene-7-chloro-9-phenyl-3,4-dihydroacridin-1(2H)-ones, 3a–j. Larvae were exposed to different concentrations of compounds, 3a–j for 24 h. All the compounds had moderate activity; maximum efficacy was observed for 3e and 3j.
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Acknowledgments
The study was supported by DST-SERB Fast Track (Sanction No. SR/FT/CS-264/2012), Government of India, New Delhi. The authors gratefully acknowledge DST-FIST for providing NMR facilities to the school. We acknowledge the support extended by VIT-SIF for GC–MS and NMR analysis.
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Bharathi, A., Mohana Roopan, S., Rahuman, A.A. et al. (E)-2-Benzylidene-7-chloro-9-phenyl-3,4-dihydroacridin-1(2H)-ones: synthesis and larvicidal activity. Res Chem Intermed 41, 2453–2464 (2015). https://doi.org/10.1007/s11164-013-1359-x
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DOI: https://doi.org/10.1007/s11164-013-1359-x