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Reversible 1,4 migration of a silyl group from oxygen to carbon: an unexpected route to α-trialkylsilyl ketoximes
Authors:J. Mora  A. Costa
Affiliation:Department of Organic Chemistry, Faculty of Sciences, University of Palma de Mallorca. Balearic Islands. Spain.
Abstract:Anions generated from trialkylsilyl ethers of methyl ketoximes (1) undergo anionic rearrangement with 1,4 migration of the silyl group. After protonation, the resulting α-trialkylsilyl ketoximes (2), suffer thermal rearrangement with 1,4 migration of the silyl group from carbon to oxygen.
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