Enehydroxylamines as versatile compounds in 3,3-sigmatropic rearrangements

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Enehydroxylamines react readily, in the presence of base, with electrophiles containing unsaturation to afford intermediates that, either spontaneously or upon heating, lead via a 3,3-sigmatropic rearrangement to α-substituted products.

Original languageEnglish
Pages (from-to)2747-2750
Number of pages4
JournalTetrahedron Letters
Issue number17
Publication statusPublished - 25 Apr 1994


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