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2-Cyanoimino-5,5-diphenyl-4-imidazolinone Monohydrate

✍ Scribed by Dupont, L. ;Masereel, B. ;Lambert, D. ;Scriba, G.


Book ID
114511938
Publisher
International Union of Crystallography
Year
1995
Tongue
English
Weight
303 KB
Volume
51
Category
Article
ISSN
0108-2701

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## Abstract The products of the addition of nucleophiles (alcohols, amines) to the cyano group of 5‐(cyanoimino)thiadiazolines 1 undergo a Boulton‐Katritzky rearrangement. The thiadiazoles 4 are formed by subsequent nitrile elimination. In the case of bicyclic thiadiazoloazepine 5 an equilibrium mi