Abstract:Cyclic β-dicarbonyl compounds 1a, 1b, 10a and 10b undergo isomerization involving reconstruction of the ring system by the UV-irradiation in strong acid media. It is suggested that the isomerization is aided by the formation of stabilized cation after the ring opening.
Die 1,3‐Cyclohexandione (Ia) und (Ib) lagem sich bei Belichtung in Fluorosulfonsäure oder 98%iger Schwefelsäure in die Dihydropyranone (IIa) und (IIb) um.
Die 1,3‐Cyclohexandione (Ia) und (Ib) lagem sich bei Belichtung in Fluorosulfonsäure oder 98%iger Schwefelsäure in die Dihydropyranone (IIa) und (IIb) um.
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