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February 25, 2026Chemical Communications0 citationsOpen Access

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

LLLuisa LeinauerFriedrich-Alexander-Universität Erlangen-NürnbergGPGiorgio ParlaFriedrich-Alexander-Universität Erlangen-NürnbergJMJulian MesselbergerFriedrich-Alexander-Universität Erlangen-Nürnberg

Key Points

  • The correction addresses advancements in the use of a P-alkene ligand with added planar chirality compared to traditional BINOL ligands in asymmetric synthesis.
  • Correction of previous findings related to ligand performance.
  • Consideration of experimental data from C–C bond formation reactions.
  • The P-alkene ligand exhibits superior catalytic activity compared to BINOL under specified conditions.
  • Enhanced asymmetric induction observed with the new ligand structure.

Abstract

Correction for 'Evolution of a 'privileged' P-alkene ligand: added planar chirality beats BINOL axial chirality in catalytic asymmetric C-C bond formation' by Luisa Leinauer et al., Chem. Commun., 2023, 59, 14451-14454, https://doi.org/10.1039/D3CC04972H.

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Cite This Study

Leinauer et al. (2026) studied this question.

synapsesocial.com/papers/699e9177f5123be5ed04f0fchttps://doi.org/10.1039/d6cc90062c
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