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Synthesis and antifungal activity of novel 2-benzimidazolylimino-5-arylidene-4-thiazolidinones
✍ Scribed by Akbar Mobinikhaledi; Naser Foroughifar; Mehdi Kalhor; Mansoureh Mirabolfathy
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 80 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.264
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✦ Synopsis
Abstract
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A series of 5‐arylidene derivatives 3a‐k, as potential antifungal agents, were synthesized in good to high yields by the reaction of 2‐benzimidazolylimino‐4‐thiazolidinone and corresponding aromatic aldehyde in a buffered medium. These compounds were evaluated for their antifungal activities against four agricultural fungi, Botrytis elliptica, Fusarium graminearum, Phytophthora nicotianae, and Rhizoctonia solani. Thereby, it was found that the compound 1 exhibits an antifungal effect against P. nicotianae and B. elliptica, comparable with carbendazim as a standard antifungal. Our results may provide some guidance for development of some novel benzimidazole‐based antifungal lead structures. J. Heterocyclic Chem., 2010.
📜 SIMILAR VOLUMES
In continuation of our studies on the synthesis and biological activity of 4-thiazolidinone~'.~), we here report the synthesis of some hydrazones and 4-thiazolidinones carrying an imidazo[ 1.2-alpyridine moiety at the Natom, prepared with the objective of screening their antifungal activities.