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Valence photoisomerization of 2H-pyrans
Authors:A. S. Dvornikov  Zh. A. Krasnaya  Ya. N. Malkin
Affiliation:(1) Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow;(2) N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow
Abstract:Conclusions 2H-Pyrans under the influence of UV light undergo reversible cleavage of the C-O bond and are isomerized to the corresponding dienones, for which reversible photochemical cis-trans isomerization around the Cagr=Cbeta bond is characteristic, and not photochemical cyclization to 2H-pyrans.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 390–394, February, 1981.The authors express their deep gratitude to V. A. Kuz'min for a valuable discussion of the study results.
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