## Abstract Treatment of 3βarylβ2βthioxoβ1,3βthiazolidinβ4βones **1** with CN^β^ and NCO^β^ effected the ring cleavage providing [(cyanocarbonothioyl)amino]benzenes **4** and arylisothiocyanates **5**, respectively. Similar treatment of 5β(2βarylβ2βoxoethyl) derivatives **2** afforded 2,4βbis(2βary
β¦ LIBER β¦
Studies on 4-thiazolidinones. VIII. The role of substituents at position-3 on the mode of cleavage of 5-Arylmethylene-2,4-dioxothiazolidines
β Scribed by Prof. Dr. M. T. Omar; M. M. Habashy; A. M. Youssef; F. A. Sherif
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 406 KB
- Volume
- 331
- Category
- Article
- ISSN
- 1615-4150
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