Journal of the Chemical Society. Chemical communications p. 124 - 125 (1985)
Update date:2022-08-05
Topics:
Graziano, M. Liliana
Scarpati, Rachele
Thermal rearrangement of the title compound (1) leads to the corresponding diepoxide (3) in apolar solvents and to the Δ2-butenolide (2) in basic solvents, whereas the formation of the epoxide (5) is independent of solvent; these conversions represent convenient entries to the syntheses of multifunctional compounds which are structurally related to biologically active products.
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