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- W1483762979 abstract "Ethenamine 1 and its methyl derivatives 2–7 have been synthesized from the adducts 8–14 by a retro-Diels-Alder reaction under flash thermolytic conditions. The primary enamines 1–4 have been identified (IR, 1H and 13C NMR) in a pure state at −80°; at the same temperature, the enamines 5–7, less stable, are already accompanied by their tautomeric imines 33 or 34. When warmed up to room temperature, the enamines 1–7 lead, following to their substitution, either to nitrogen heterocycles (30, 42) or to acyclic azadienes (35–37, 39, 40)." @default.
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- W1483762979 date "1980-01-01" @default.
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- W1483762979 title "Reactions retrodieniques—IX" @default.
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