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- W2315462893 abstract "Mannich bases were prepared from substituted phenols with aliphatic amines and formaldehyde. Amine exchange with N-methyl-2-naphthylamine followed by a Hofmann Martius rearrangement gave rise to o,o′-amino-hydroxy-diphenylmethane derivatives. Under cyclization conditions some of these compounds produced spirocyclohexadienones, which are the ipso analogs to the hypothetic intermediates postulated in the aminomethylation mechanism of phenols." @default.
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- W2315462893 date "1995-12-01" @default.
- W2315462893 modified "2023-10-03" @default.
- W2315462893 title "Heterocyclische Spirocyclohexadienone aus substituierten Phenolen / Heterocyclic Spirocyclohexadienones from Substituted Phenols" @default.
- W2315462893 doi "https://doi.org/10.1515/znb-1995-1213" @default.
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