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Gold-Catalyzed Tandem [3,3]-Propargyl Ester Rearrangement Leading to (E)‑1H‑Inden-1-ones

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journal contribution
posted on 03.01.2014, 00:00 authored by Li-Jing Wang, Hai-Tao Zhu, An-Qi Wang, Yi-Feng Qiu, Xue-Yuan Liu, Yong-Min Liang
An efficient method for the synthesis of (E)-1H-inden-1-ones using gold-catalyzed tandem [3,3]-propargyl ester rearrangement followed by Michael addition under mild reaction conditions has been developed. The resulting products are important frameworks found in numerous natural products and pharmaceutically active compounds, as well as being valuable intermediates in organic synthesis.

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