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- W2160999315 abstract "Au-spicious! Under silver-free conditions, simple 3-silyloxy-1,5-enynes were converted into complex cyclopentenes by a gold(I)-catalyzed sequence that likely proceeds through a carbocyclization followed by a pinacol rearrangement. For the final demetalation step, isopropyl alcohol and N-iodosuccinimide are effectively utilized, and the resulting products are set up for a wealth of further reactions. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2007/z604544_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W2160999315 created "2016-06-24" @default.
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- W2160999315 date "2007-03-19" @default.
- W2160999315 modified "2023-10-02" @default.
- W2160999315 title "Catalyzed Tandem Reaction of 3-Silyloxy-1,5-enynes Consisting of Cyclization and Pinacol Rearrangement" @default.
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- W2160999315 doi "https://doi.org/10.1002/anie.200604544" @default.
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