Gold-Catalyzed Diastereoselective Synthesis of alpha-Fluoroenones from Propargyl Acetates
A diastereoselective preparation of -fluoroenones from propargyl acetates has been developed proceeding via a gold-catalyzed rearrangement-fluorination cascade. Control reactions are consistent with a mechanism involving a gold-mediated 3,3-sigmatropic shift followed by a direct, nongold-catalyzed e...
Главные авторы: | Hopkinson, M, Giuffredi, G, Gee, A, Gouverneur, V |
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Формат: | Journal article |
Язык: | English |
Опубликовано: |
2010
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