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article · Chemical Communications

Evolution of a ‘privileged’ P-alkene ligand: added planar chirality beats BINOL axial chirality in catalytic asymmetric C–C bond formation

Abstract

)-5 form optically pure complexes of Rh(I) and Pd(II), which catalyze conjugate additions of boron C-nucleophiles to enones and allylic alkylations, respectively. In the Rh-catalyzed reaction, the planar chirality of the alkene exerts absolute enantiocontrol over the potent BINOL auxiliary.

Research topics

  • Axial and Atropisomeric Chirality Synthesis
  • Asymmetric Synthesis and Catalysis
  • Molecular spectroscopy and chirality

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DOI: 10.1039/d3cc04972h

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