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HERO ID
6134121
Reference Type
Journal Article
Title
Heterocyclische Spirocyclohexadienone aus substituierten Phenolen / Heterocyclic Spirocyclohexadienones from Substituted Phenols
Author(s)
Möhrle, H; Schake, D
Year
2014
Publisher
Verlag der Zeitschrift für Naturforschung
Book Title
Zeitschrift für Naturforschung B
Volume
50, no. 12
Page Numbers
1859-1868
DOI
10.1515/znb-1995-1213
URL
http://dx.doi.org/10.1515/znb-1995-1213 Available from publisher's site
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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.
Keywords
amines; aminomethylation; formaldehyde; phenols; Internet resource
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