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A stable enol from a 6-substituted benzanthrone and its unexpected behaviour under acidic conditions
Treatment of benzanthrone (1) with biphenyl-2-yl lithium leads to the surprisingly stable enol 4, which is converted by dehydrogenation into the benzanthrone derivative 7. Under acidic conditions 4 isomerises to the spiro compound 11 and the bicyclo[4.3.1]decane derivative 12. Furthermore, the forma...
Autores principales: | Debeaux, Marc, Brandhorst, Kai, Jones, Peter G, Hopf, Henning, Grunenberg, Jörg, Kowalsky, Wolfgang, Johannes, Hans-Hermann |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2707016/ https://www.ncbi.nlm.nih.gov/pubmed/19597557 http://dx.doi.org/10.3762/bjoc.5.31 |
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