期刊
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 65, 期 -, 页码 295-303出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2013.04.061
关键词
One pot synthesis; Substituted benzo[d]thiazole; 2-Naphthol; 6-Hydroxyquinoline; Microwave irradiation; Single crystal X-ray studies; Larvicide; Insecticide; Adulticidal activity; Repellent
资金
- NRF South Africa
A novel and efficient one pot synthesis was developed for 2,6-substituted-benzo[d]thiazole analogues 4a -k and 2,4-substituted-benzo[d]thiazole analogues 41 p via three component condensation reaction of substituted arylaldehyde, 2-amino-6-halo/4-methyl-benzo[d]thiazole and 2-naphthol or 6-hydroxy quinoline in presence of 10% w/v NaCl in water by microwave method. This method enabled for short reaction times, easy work-up and significant high yields. The title compound 4b was used for single crystal X-ray studies in order to understand its conformation and packing features. The title compounds 4a p were screened for antimosquito properties such as repellency, insecticidal and larvicidal activity against Anopheles arabiensis by mosquito feeding-probing assay, cone bio-assay and standard WHO larvicidal assay, respectively. Among these analogous 4b, 4d and 4p exhibit the highest repellent activity comparable to the positive control DEET, and 4a and 4k knockdown most mosquitoes on repellent assays. (C) 2013 Elsevier Masson SAS. All rights reserved.
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