A catalytic enantiotopic-group-selective Suzuki reaction for the construction of chiral organoboronates

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Abstract

Catalytic enantiotopic-group-selective cross-couplings of achiral geminal bis(pinacolboronates) provide a route for the construction of nonracemic chiral organoboronates. In the presence of a chiral monodentate taddol-derived phosphoramidite ligand, these reactions occur with high levels of asymmetric induction. Mechanistic experiments with chiral 10B-enriched geminal bis(boronates) suggest that the reaction occurs by a stereochemistry-determining transmetalation that occurs with inversion of configuration at carbon. © 2014 American Chemical Society.

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Sun, C., Potter, B., & Morken, J. P. (2014). A catalytic enantiotopic-group-selective Suzuki reaction for the construction of chiral organoboronates. Journal of the American Chemical Society, 136(18), 6534–6537. https://doi.org/10.1021/ja500029w

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