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- W2951522562 abstract "The photoreactions of α,β-unsaturated γ,δ-epoxy nitriles 1, 2, 13 and 16 with triethylamine give rise to novel 1 ∶ 1 α-adducts (e.g., 5) efficiently. After treatment with silica gel, the adducts undergo retro-Michael reaction leading to the corresponding α-alkylidenenitrile derivatives (e.g., 3). The epoxy nitrile 1 also reacts with various tertiary amines to afford α-adducts. The reaction of 1 and the silylamine 24 gives mainly methylene derivative 22 and silylated compound 25after treatment with silica gel. The reaction may proceed via single- electron-transfer from the amine to the excited epoxy nitrile." @default.
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- W2951522562 date "2003-02-04" @default.
- W2951522562 modified "2023-09-27" @default.
- W2951522562 title "Novel Photoadditions of Tertiary Amines to the α-Position of α,β-Unsaturated γ,δ-Epoxy Nitriles." @default.
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- W2951522562 doi "https://doi.org/10.1002/chin.200305076" @default.
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