Published January 1, 2012
| Version v1
Journal article
Open
Synthesis and anti-protozoal activity of novel dihydropyrrolo[3,4-d][1,2,3]triazoles
- 1. Abant Izzet Baysal Univ, Dept Chem, TR-14280 Bolu, Turkey
- 2. Swiss Trop & Publ Hlth Inst, Dept Med Parasitol & Infect Biol, CH-4002 Basel, Switzerland
- 3. Univ London, Dept Pharmaceut & Biol Chem, Ctr Pharmacognosy & Phytotherapy, Sch Pharm, London WC1N 1AX, England
Description
1,2,4-Oxadiazole and 1,2,3-triazole containing heterocyclic compounds continue to gain interest in synthesis of chemical entities and exhibit various biological activities as anti-protozoal and anti-cancer agents. By using the principle of bioisosterism, a series of novel oxadiazolyl pyrrolo triazole diones; namely, (3aS,6aR)-1-((3-(4-substituted phenyl)-1,2,4-oxadiazol-5-yl)methyl)-5-phenyl-1,6a-dihydropyrrolo[3,4-d][1,2,3] triazole-4,6(3aH,5H)-diones (5a-k) was designed and synthesized by the 1,3-dipolar cycloaddition reaction of novel 5-azidomethyl 3-aryl substituted 1,2,4-oxadiazoles (4a-k) with N-phenyl maleimide. The structures of all the cycloadducts were elucidated by means of spectroscopic methods and physical characteristics. The in vitro anti-protozoal and cytotoxic activities of these novel heterocyclic compounds were investigated. (C) 2011 Elsevier Masson SAS. All rights reserved.
Files
bib-57550203-1579-4e9d-8e48-99ddac755f68.txt
Files
(204 Bytes)
| Name | Size | Download all |
|---|---|---|
|
md5:2ce7b0c6fe6601335c62faeb95cf2160
|
204 Bytes | Preview Download |