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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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