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    Gold-Catalyzed Oxime-Oxime Rearrangement
    (Amer Chemical Soc, 2015) Guven, Sinem; Ozer, Merve Sinem; Kaya, Serdal; Menges, Nurettin; Balci, Metin
    The gold-catalyzed reaction of pyrrole and indole oximes having a propargyl group attached to the nitrogen atom was studied. The selective 6-endo-dig mode of cyclization was observed for the terminal alkynes giving rise to the formation of pyrazine N-oxides in the presence of a gold catalyst. However, the reaction with substituted alkyne transferred the oxime functionality intramolecularly from one carbon atom to another via the 7-endo-dig cyclization process. This transformation is unprecedented in the literature and is named an oximeoxime rearrangement.