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- W2034972988 endingPage "243" @default.
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- W2034972988 abstract "Derivatives of 1,2-dioxacyclohex-4-ene and 2,3-dioxabicyclo[2.2.2]oct-5-ene (endoperoxides, EPs) form EDA complexes with tetracyanoethylene (TCNE). The phenyl-substituted EPs 3a, 4a, 4b, and 6 undergo electron-transfer-induced reactions when the EDA complexes are irradiated. Two types of reactions are observed depending on the ring system. Monocyclic EPs (3a, 4a, and 4b) afford furan derivatives, possibly through the Criegee-type rearrangement, and dehydration, whereas the bicyclic EP 6 undergoes cycloreversion through the C–O cleavage." @default.
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- W2034972988 date "1993-01-01" @default.
- W2034972988 modified "2023-10-17" @default.
- W2034972988 title "Electron-transfer photochemistry of endoperoxides" @default.
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- W2034972988 doi "https://doi.org/10.1039/p29930000243" @default.
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