The Reaction of Cyanothioformamide with Isocyanates − Formation of a Disulfide by Reduction of a Thiocarbonyl Group
✍ Scribed by Roger Ketcham; Ernst Schaumann; Gunadi Adiwidjaja
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 282 KB
- Volume
- 2001
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
The reactions of the title compounds are governed by sulfur redox chemistry. Thus, cyanothioformamide 2 reacts with aryl isocyanates 3a-c to give bis[3-aryl-1-(arylcarbamoyl)-2oxo-4-(arylcarbamoylimino)imidazolidin-5-yl] disulfides 6, as shown by an X-ray crystallographic investigation of product 6a. Reaction with methyl isocyanate (3d) gives the related [ ‡] Heterocyclic Ring-Closure Reactions, Part XI. Ϫ Part X: Ref.
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