Abstract
Photolysis of 2-Phenyl-4-ethylidene-5(4H)-oxazolones in the presence of allylic alcohols resulted in a navel one-pot transformation to γ,δ- unsaturated N-benzoyl amides via decarbonylation, nucleophilic addition of allylic alcohols, photoinduced hydrogen transfer and the Claisen rearrangement.
Original language | English |
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Pages (from-to) | 9711-9714 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 39 |
Issue number | 52 |
DOIs | |
State | Published - 24 Dec 1998 |