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- W2521572012 abstract "Photolyses of flavanone and substituted flavanones in benzene led to the cleavage of the pyrone ring to give corresponding 2′-hydroxychalcones, while similar irradiation of flavanone or 4-chromanone in 2-propanol gave coupling products (pinacols and solvent adducts). However, photolysis of 7,8-benzoflavanone in 2-propanol led to the cleavage of the pyrone ring instead of the formation of coupling products. It is implied that the cleavage of the pyrone ring takes place via π-π* triplet states, while formation of coupling products via n-π* triplet states." @default.
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- W2521572012 date "1976-06-05" @default.
- W2521572012 modified "2023-09-25" @default.
- W2521572012 title "PHOTOREACTIONS VIA π-π*ANDn-π*TRIPLET STATES OF FLAVANONES" @default.
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- W2521572012 doi "https://doi.org/10.1246/cl.1976.579" @default.
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