Synthesis of Aromatic Ketones by a Transition Metal Catalyzed Tandem Sequence

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2006

Other naphthalene derivativesQ 1020 Synthesis of Aromatic Ketones by a Transition Metal Catalyzed Tandem

Sequence. — The target compounds are prepared through the metal-catalyzed [3,3]-sigmatropic rearrangement/formal Myers—Saito cyclization of various propar-gylic esters. — (ZHAO, J.; HUGHES, C. O.; TOSTE*, F. D.; J. Am. Chem. Soc. 128 (2006) 23, 7436-7437; Dep. Chem., Univ. Calif., Berkeley, CA 94720, USA; Eng.) — Y. Steudel

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Synthesis of Aromatic Ketones by a Transition Metal Catalyzed Tandem Sequence

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