Enantioselective Access to Triaryl-2-pyrones with Monoaxial or Contiguous C–C Diaxes via Oxidative NHC Catalysis

We present herein an unprecedented stereoselective synthesis of triaryl-2-pyrones with monoaxial or contiguous diaxes from readily available starting materials. This N-heterocyclic carbene catalysis method adopts an atroposelective annulation of 2-aryketones with ynals under oxidative conditions. Th...

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Veröffentlicht in:ACS catalysis 2023-02, Vol.13 (4), p.2565-2575
Hauptverfasser: Zhang, Si-Chen, Liu, Shengping, Wang, Xia, Wang, Shao-Jie, Yang, Hui, Li, Lin, Yang, Binmiao, Wong, Ming Wah, Zhao, Yu, Lu, Shenci
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Sprache:eng
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Zusammenfassung:We present herein an unprecedented stereoselective synthesis of triaryl-2-pyrones with monoaxial or contiguous diaxes from readily available starting materials. This N-heterocyclic carbene catalysis method adopts an atroposelective annulation of 2-aryketones with ynals under oxidative conditions. The annulation includes the construction of one or two axes in a single operation, achieves step economy, and affords axially chiral triaryl-2-pyrones in moderate to good yields, with high to excellent enantioselectivities. DFT calculations of the relative energies of stereoisomers and rotational barriers were performed.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.2c05570