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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Doi:10.1021/om00092a007
(1988)Doi:10.1002/chem.200802146
(2008)Doi:10.1002/ardp.19873200315
(1987)Doi:10.1016/j.tet.2008.10.090
(2009)Doi:10.1016/S0040-4020(01)88114-X
(1986)Doi:10.1002/ardp.200800004
(2008)
