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Published on: August 6, 2018
Deprotonation of Benzoxazolium Salt: Trapping of a Radical-Cation Intermediate
Svetlana V Klementyeva1, Pavel A Abramov2,3, Nikolay V Somov4
1Kazan Federal University , A.M. Butlerov Institute of Chemistry , 420008 , Kremlevskaya str. 29/1 , Kazan , Russian Federation.
Abstract:
The deprotonation of N-2,6-diisopropylphenyl-substituted benzoxazolium tetrafluoroborate 1 with NaH results in the formation of electron-rich diaminodioxaethylene 2. The radical cation salt 2·+·BF4- is found to be an intermediate product in the redox reaction leading from 1 to 2.
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