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. 2010 Jun 18;12(12):2806-9.
doi: 10.1021/ol100895d.

Diversity-oriented synthesis of disubstituted alkenes using masked silanols

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Diversity-oriented synthesis of disubstituted alkenes using masked silanols

Hannah F Sore et al. Org Lett. .

Abstract

The regio- and stereoselective synthesis and subsequent Hiyama cross coupling of pentafluorophenyldimethylvinylsilanes has been developed, thus providing a convenient and robust method for the diversity-oriented synthesis of (E)-, (Z)- and alpha-disubstituted alkenes from terminal alkynes. Pentafluorophenyldimethylvinylsilanes undergo cross-coupling reactions with excellent selectivity and in good yields, offering an attractive alternative to existing masked silanols.

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