Oxadiazole mannich bases: Synthesis and antimycobacterial activity
MA Ali, M Shaharyar
Index: Ali, Mohamed Ashraf; Shaharyar, Mohammad Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 12 p. 3314 - 3316
Full Text: HTML
Citation Number: 133
Abstract
A series of oxadiazole mannich bases were synthesized by reacting oxadiazole derivatives, dapsone and appropriate aldehyde in the presence of methanol. The synthesized compounds were evaluated for antimycobacterial activity against M. tuberculosis H37Rv and INH resistant M. tuberculosis. Among the synthesized compounds, compound (4) 3-{2-furyl [4-(4-{2-furyl [5-(2-naphthyloxymethyl)-2-thioxo-2, 3-dihydro-1, 3, 4-oxadiazol-3-yl] ...
Related Articles:
SYNTHESIS AND IN VITRO SEROTONIN-3-ANTAGONIST ACTIVITIES OF SOME NEWER 1, 3, 4-OXADIAZOLE-2-THRONES
[Pramanik, S. S.; Mukherjee, A. Journal of the Indian Chemical Society, 1998 , vol. 75, # 1 p. 53 - 54]
SYNTHESIS AND IN VITRO SEROTONIN-3-ANTAGONIST ACTIVITIES OF SOME NEWER 1, 3, 4-OXADIAZOLE-2-THRONES
[Pramanik, S. S.; Mukherjee, A. Journal of the Indian Chemical Society, 1998 , vol. 75, # 1 p. 53 - 54]
The condensation of carboxylic acid hydrazides with carbon disulfide
[Ainsworth Journal of the American Chemical Society, 1956 , vol. 78, p. 4475,4476]
SYNTHESIS AND IN VITRO SEROTONIN-3-ANTAGONIST ACTIVITIES OF SOME NEWER 1, 3, 4-OXADIAZOLE-2-THRONES
[Pramanik, S. S.; Mukherjee, A. Journal of the Indian Chemical Society, 1998 , vol. 75, # 1 p. 53 - 54]