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Published on: July 23, 2016
Synthesis of aromatic ketones by a transition metal-catalyzed tandem sequence
Jing Zhao1, Colin O Hughes, F Dean Toste
1Department of Chemistry, University of California, Berkeley, California 94720, USA.
Abstract:
Both simple Ag(I) and Au(I) are effective catalysts for a tandem [3,3]-sigmatropic rearrangement/formal Myers-Saito cyclization of propargyl esters to form aromatic ketones. A mechanism in which the metal catalyzes both of these processes through alkyne activation is proposed. By using this method a wide range of aromatic structures including naphthyl, anthracenyl and indole ketones are available from readily available propargyl esters.
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