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Published on: November 9, 2019
Cucurbit[7]uril-Catalyzed Beckmann Rearrangement of Arylketoximes
Dechao Liu1, Ying Fan1,2, Mao Liu1,2,3
1Enterprise Technology Center of Guizhou Province, Guizhou University, Guiyang 550025, People's Republic of China.
Abstract:
With the existence of cucurbit[7]uril (Q[7]), a supramolecular catalysis strategy for the Beckmann rearrangement of aryl ketoximes to N-substituted amides was successfully established. The cavity of Q[7] was found to be essential for substrate encapsulation and the rearrangement reaction through comparative experiments and studies on host-guest interactions. This supramolecular strategy provides an efficient route for the rearrangement reaction incorporating a carbonation intermediate.
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