The first examples of the enantioselective Heck-Matsuda reaction: arylation of unactivated cyclic olefins using chiral bisoxazolines
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摘要
Successful enantioselective Heck-Matsuda arylations were accomplished for the first time using chiral bisoxazolines as ligands. Enantioselective Heck arylations were performed with several cyclic nonactivated olefins to provide the Heck products in 63-96%isolated yields and in enantiomeric excesses of 54%up to 84%.

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