Abstract
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 language | English |
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Pages (from-to) | 2747-2750 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 35 |
Issue number | 17 |
DOIs | |
Publication status | Published - 25 Apr 1994 |