## Abstract Treatment of 3‐aryl‐2‐thioxo‐1,3‐thiazolidin‐4‐ones **1** with CN^−^ and NCO^−^ effected the ring cleavage providing [(cyanocarbonothioyl)amino]benzenes **4** and arylisothiocyanates **5**, respectively. Similar treatment of 5‐(2‐aryl‐2‐oxoethyl) derivatives **2** afforded 2,4‐bis(2‐ary
✦ LIBER ✦
A comparative esr study of the reactions of group ivb organometallic radicals with 4,4′-dimethoxybenzophenone, 4,4′-dimethoxythiobenzophenone, and 3-ethyl-2-thioxo-4-oxazolidione
✍ Scribed by Babatunde B. Adeleke; Kuang S. Chen; Jeffrey K.S. Wan
- Book ID
- 108347067
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 690 KB
- Volume
- 208
- Category
- Article
- ISSN
- 0022-328X
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