An efficient one-pot cyclization of quinoline thiosemicarbazones to quinolines derivatized with 1,3,4-thiadiazole as anticancer and anti-tubercular agents
摘要:
A series of 6,7,8-substituted thiosemicarbazones (2a-j) of 2-chloro-3-formyl-quinoline derivatives were cyclized to the title compounds (3a-j) using acetic anhydride. The structures of the final compounds (3a-j) were confirmed by elemental and spectral (IR, H-1 NMR and MS) analysis. Some of the title compounds have shown promising anticancer and antitubercular activities.
Efficient reduction of graphene oxide to graphene nanosheets using a silica-based ionic liquid: synthesis, characterization and catalytic properties of IMD-Si/FeCl4−@GNS
Efficient reduction of graphene oxide to graphene nanosheets using a silica-based ionic liquid: synthesis, characterization and catalytic properties of IMD-Si/FeCl<sub>4</sub><sup>−</sup>@GNS
作者:Mohd Umar Khan、Shaheen Siddiqui、Waqas Ahmad Khan、Zeba N. Siddiqui
DOI:10.1039/c9nj05768d
日期:——
Ionic liquid-modified graphene nanosheets (IMD-Si/FeCl4−@GNS) have been synthesized as efficient catalysts for the synthesis of (E)-selective thiosemicarbazones.
An efficient one-pot cyclization of quinoline thiosemicarbazones to quinolines derivatized with 1,3,4-thiadiazole as anticancer and anti-tubercular agents
作者:Sheetal B. Marganakop、Ravindra R. Kamble、Tasneem Taj、Mahadevappa Y. Kariduraganvar
DOI:10.1007/s00044-010-9522-z
日期:2012.2
A series of 6,7,8-substituted thiosemicarbazones (2a-j) of 2-chloro-3-formyl-quinoline derivatives were cyclized to the title compounds (3a-j) using acetic anhydride. The structures of the final compounds (3a-j) were confirmed by elemental and spectral (IR, H-1 NMR and MS) analysis. Some of the title compounds have shown promising anticancer and antitubercular activities.