Microwave-assisted green synthesis of new imidazo[2,1-b]thiazole derivatives and their antimicrobial, antimalarial, and antitubercular activities
@article{Vekariya2017MicrowaveassistedGS, title={Microwave-assisted green synthesis of new imidazo[2,1-b]thiazole derivatives and their antimicrobial, antimalarial, and antitubercular activities}, author={Rajesh H. Vekariya and Kinjal D. Patel and Mayur K. Vekariya and Neelam P. Prajapati and Dhanji P. Rajani and Smita D. Rajani and Hitesh D. Patel}, journal={Research on Chemical Intermediates}, year={2017}, volume={43}, pages={6207-6231} }
We have synthesized some imidazo[2,1-b]thiazole derivatives by reaction of 1-(2-amino-4-methylthiazol-5-yl)ethanone or ethyl 2-amino-4-methylthiazole-5-carboxylate with α-bromo aralkyl ketones (phenacyl bromides) in presence of polyethylene glycol-400 (PEG-400) as efficient, inexpensive, biodegradable, and green reaction medium and catalyst (dual nature) under Microwave Irradiation (MWI) at 300 W as well as under thermal heating at 90 °C. Moreover, we also synthesized 1-(2-amino-4-methylthiazol…
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References
SHOWING 1-10 OF 60 REFERENCES
Microwave assisted synthesis of novel imidazo [2,1-b]thiazole derivative attached to quinoxalinones
- Chemistry
- 2012
Synthesis and antimicrobial studies of novel methylene bridged benzisoxazolyl imidazo[2,1-b][1,3,4]thiadiazole derivatives.
- ChemistryEuropean journal of medicinal chemistry
- 2009
A one pot, three component synthesis of coumarin hybrid thiosemicarbazone derivatives and their antimicrobial evolution
- Chemistry
- 2017
Synthesis and antimicrobial activity evaluation of new 1,2,4-triazoles and 1,3,4-thiadiazoles bearing imidazo[2,1-b]thiazole moiety.
- ChemistryEuropean journal of medicinal chemistry
- 2010
Synthesis and anti-inflammatory evaluation of methylene bridged benzofuranyl imidazo[2,1-b][1,3,4]thiadiazoles.
- ChemistryEuropean journal of medicinal chemistry
- 2008
Synthesis and antimicrobial activities of some ethyl 2-arylthio-6-arylimidazo[2,1-b]thiazole-3-carboxylates and their sulfones
- Chemistry
- 2008
A series of new 2-arylthio-3-ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles (4a–4h) and 2-arenesulfonyl-3-ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles (5a–5h) have been prepared and characterized by…
Potential antitumor agents. 37. Synthesis and antitumor activity of guanylhydrazones from imidazo[2,1-b]thiazoles and from the new heterocyclic system thiazolo[2',3':2,3]imidazo[4,5-c]quinoline.
- ChemistryJournal of medicinal chemistry
- 2005
The effect of the guanylhydrazone of 2-chloro-6-(2,5-dimethoxy-4-nitrophenyl)imidazo[2,1-b]thiazole-5-carbaldehyde was investigated, and it was found to be an inhibitor of Complex III of the mitochondrial respiratory chain and is able to induce apoptosis in the cell lines HT29 and HL60.
Synthesis and primary cytotoxicity evaluation of new imidazo[2,1-b]thiazole derivatives.
- ChemistryEuropean journal of medicinal chemistry
- 2007
Antitumor activity of new substituted 3-(5-imidazo[2,1-b]thiazolylmethylene)-2-indolinones and 3-(5-imidazo[2,1-b]thiadiazolylmethylene)-2-indolinones: selectivity against colon tumor cells and effect on cell cycle-related events.
- Chemistry, BiologyJournal of medicinal chemistry
- 2008
Its ability to inhibit cellular proliferation was mediated by cell cycle arrest at the G2/M phase, accompanied by inhibition of ornithine decarboxylase (ODC), the limiting enzyme of polyamine synthesis, and followed by induction of apoptosis.