Oxime derivatives as a-electrophiles. from a-tetralone oximes to tetracyclic frameworks

Abstract : When subjected to the conditions of a Semmler-Wolff/Schroeter aromatization, the oximes of 4-benzyl-substituted tetralones undergo an electrophilic aromatic substitution reaction to form tetracyclic frameworks. © 2011 American Chemical Society.
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Béatrice Quiclet-Sire, Nina Tölle, Syeda Zafar, Samir Zard. Oxime derivatives as a-electrophiles. from a-tetralone oximes to tetracyclic frameworks. Organic Letters, American Chemical Society, 2011, 13 (12), pp.3266-3269. ⟨10.1021/ol2012204⟩. ⟨hal-00951231⟩

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