Synthesis and biological activities of 2-alkylthio-5-furylmethylidene-4H-imidazolin-4-ones
✍ Scribed by Feng-Ling Yang; Zhao-Jie Liu; Xiao-Bo Huang; Ming-Wu Ding
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2004
- Tongue
- English
- Weight
- 278 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Novel 2‐alkylthio‐5‐furylmethylidene‐4__H__‐imidazolin‐4‐ones 4 have been synthesized via tandem aza‐ Wittig reaction. The structures were determined by ir, nmr, mass spectroscopy, and elemental analysis. They were screened for fungicidal activities against Fusarium oxysporium, Botryosphaeria berengeriana and Rhizoctonia solani, and growth inhibition of Barnyard grass and Cole root and stalk. A few of them possess significant biological activities.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract 2‐Alkylthio‐5‐phenylmethylidene‐4H‐imidazol‐4‐ones **__4__** were synthesized by S‐alkylation of 2‐thioxo‐3‐alkyl(aryl)‐4‐imidazolidinones **__3__**, which were obtained via cyclization of isothiocyanates **__2__** with aliphatic(aromatic) primary amines. © 2003 Wiley Periodicals, Inc.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.