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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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https://hal-polytechnique.archives-ouvertes.fr/hal-00951231
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Submitted on : Thursday, February 27, 2014 - 10:18:34 AM
Last modification on : Thursday, December 9, 2021 - 2:26:02 PM

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Béatrice Quiclet-Sire, Nina Tölle, Syeda N. Zafar, Samir Z. 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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