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Enynones in organic synthesis. I. Spiroannulation by tandem oxy-cope rearrangement-electrocyclic ring closure
Authors:Peter A Jacobi    Lisa M Armacost  Joseph I Kravitz  Michael J Martinelli  Harold G Selnick
Institution:

Hall-Atwater Laboratories, Wesleyan University Middletown, Connecticut 06457 U.S.A.

Abstract:Bis-acetylenic alcohols of proper design undergo a facile oxy-Cope rearrangement to afford mixtures of E- and Z-enynones. These latter compounds afford methylenecyclopentenones upon enolization and electrocyclic ring closure.
Keywords:
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