dc.contributor.author |
Audichya, Vipul B. |
|
dc.contributor.author |
Savant, Mahesh M. |
|
dc.contributor.author |
Naliapara, Yogesh T. |
|
dc.date.accessioned |
2021-08-19T10:31:37Z |
|
dc.date.available |
2021-08-19T10:31:37Z |
|
dc.date.issued |
2017-02-08 |
|
dc.identifier.citation |
Audichya, V. B., Savant, M. M., & Naliapara, Y. T. (2017). SYNTHESIS OF NOVEL SUBSTITUTED 2H-THIAZOLO [3, 2-a] PYRIMIDINES USING WATER AS GREEN SOLVENT AND THEIR ANTIMICROBIAL EVALUATION. World Journal of Pharmacy and Pharmaceutical Sciences, 6(3), 775-786. |
en_US |
dc.identifier.issn |
2278–4357 |
|
dc.identifier.uri |
https://www.wjpps.com/Wjpps_controller/abstract_id/6738 |
|
dc.identifier.uri |
http://10.9.150.37:8080/dspace//handle/atmiyauni/710 |
|
dc.description.abstract |
A novel series of N,5-bis(4-fluorophenyl)-3,5-dihydro-7-isopropyl-2H-thiazolo[3,2-a]pyrimidine -6-carboxamide has been prepared by reaction of N,4-bis(4-fluorophenyl)-1,2,3,4-tetrahydro-6-isopropyl-2-thioxopyrimidine-5-carboxamide with dibromoethane using basic catalysts TEA/ K2CO3, in the presence of TBAB/TEAB in water. We found water as an efficient and green solvent for the synthesis of novel thiazolo [3,2-a] pyrimidine scaffolds in good yields for biological interest. Among all compounds, 8c, 8g, 8i, 8l and 8o shows good antimicrobial activity against bacterial strain compare to ciprofloxacin. |
en_US |
dc.language.iso |
en_US |
en_US |
dc.publisher |
World Journal of Pharmacy and Pharmaceutical Sciences |
en_US |
dc.subject |
Thiazolo[3,2-a]pyrimidine, Pyrimidine, Alkylation Antimicrobial evaluation. |
en_US |
dc.title |
Synthesis Of Novel Substituted 2h-Thiazolo [3,2-A] Pyrimidines Using Water As Green Solvent And Their Antimicrobial Evaluation |
en_US |
dc.type |
Article |
en_US |