Abstract:
Condensation of α,β-unsaturated β-dimethylaminoaldehydes with heptane-2,4,6-trione unexpectedly affords a new type of substituted phenols (4a–c; 5a,c) due to intramolecular cyclization accompanied by 1,6-deamination.
Document Type:
Article
Language: English
Citation:
Zh. A. Krasnaya, E. V. Grechkina, V. S. Bogdanov, “Synthesis of Novel Substituted Phenols by Condensation of α,β-Unsaturated β-Dimethylaminoaldehyde Aminals with Triketones”, Mendeleev Commun., 3:5 (1993), 195–196
Linking options:
https://www.mathnet.ru/eng/mendc5328
https://www.mathnet.ru/eng/mendc/v3/i5/p195
This publication is cited in the following 2 articles:
Graham Smith, “The Ethnic Democracy Thesis and the Citizenship Question in Estonia and Latvia”, Natl. pap., 24:2 (1996), 199
Z. A. KRASNAYA, E. V. GRECHKINA, V. S. BOGDANOV, “ChemInform Abstract: Synthesis of Novel Substituted Phenols by Condensation of α,. beta.‐Unsaturated β‐Dimethylaminoaldehyde Aminals with Triketones.”, ChemInform, 25:15 (1994)
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