Synthesis and anti-Helicobacter pylori activity of 4-(coumarin-3-yl)thiazol-2-ylhydrazone derivatives
β Scribed by Franco Chimenti; Bruna Bizzarri; Adriana Bolasco; Daniela Secci; Paola Chimenti; Arianna Granese; Simone Carradori; Melissa D'Ascenzio; M. Maddalena Scaltrito; Francesca Sisto
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 99 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.464
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
magnified image A novel class of coumarinβthiazole conjugated systems (1β31) were synthesized by Hantzsch condensation between Ξ±βbromoβ3βacetyl coumarin and several thiosemicarbazone intermediates. This scaffold was also evaluated for selective antibacterial activity against 20 isolates of H. pylori clinical strains, including four metronidazole resistant ones. J. Heterocyclic Chem., (2010).
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Photohalogenation of 3-Acetylcoumarins: Facile Synthesis of 3-(2-Amino-4-thiazolyl)coumarins and Their Conversion into 3-[2-(2,5-Dimethylpyrrol-1-yl)thiazol-4-yl]coumarins. -A facile synthesis of 3-(2-amino-4-thiazolyl)coumarins (III) by reacting acetylcoumarins (I) with thiourea under photohalogen