SCHEDULED MAINTENANCE
Allyl alcohol reacts with 1-heteroaryl-3-oxidopyridiniums to give a tricyclic product (10) in which the OH group has added to the αβ-unsaturated ketone. Analogous products are obtained from N-allylbenzenesulphonamide, acrylic acid, and 2-vinylpyridine. Further transformations of the primary adducts are described.
A. R. Katritzky, N. Dennis, G. J. Sabongi and L. Turker, J. Chem. Soc., Perkin Trans. 1, 1979, 1525 DOI: 10.1039/P19790001525
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