
Journal of the American Chemical Society p. 3784 - 3793 (1980)
Update date:2022-08-04
Topics:
Nicolaou, K. C.
Magolda, R. L.
Sipio, W. J.
Barnette, W. E.
Lysenko, Z.
Joullie, M. M.
Phenylselenoetherification, a new cyclization procedure based on organoselenium chemistry, is described in detail.Unsaturated hydroxy and thio compounds were subjected to this new cyclization process to afford a series of phenyl selenoethers and phenyl selenothioethers which were transformed to a variety of heterocyclic systems by reductive or oxidative removal of the selenium group.Applications to the synthesis of muscarine analogues are described.
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