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April 10, 2026ACS Catalysis1 citations

Atroposelective Synthesis of Axially Chiral Styrenes by Dual Photoredox/Copper-Catalyzed Carbocyanation of Alkynes

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YCYa-Sheng CaoLaboratoire de Synthèse OrganiqueYHYuan HuJingdezhen Ceramic InstituteWGWanru GuoLaboratoire de Synthèse Organique

Key Points

  • The study aims to develop a reliable method for synthesizing axially chiral styrenes using photoredox and copper catalysis.
  • Utilized a dual photoredox/copper-catalyzed approach.
  • Converted N-hydroxyphthalimide esters and 2-aminoaryl alkynes to styrene atropisomers.
  • Conducted reactions under redox-neutral conditions.
  • Examined enantioselectivity and E-selectivity in products.
  • Achieved high yields of styrene atropisomers.
  • Demonstrated high enantioselectivity and E-selectivity.
  • Successfully scaled up reactions for practical applications.
  • Enabled versatile transformations of the synthesized products.

Abstract

The atroposelective synthesis of axially chiral styrenes remains a formidable challenge due to the configurational lability and the difficulty in controlling alkene geometry. Herein, we report a synergistic photoredox/copper-catalyzed carbocyanation of terminal alkynes that enables efficient access to these valuable scaffolds. Under redox-neutral conditions, a wide range of readily available N-hydroxyphthalimide esters and 2-aminoaryl alkynes are efficiently converted into the corresponding styrene atropisomers in good yields with high enantioselectivity and E-selectivity. The practicality of this method is highlighted by successful scale-up reactions and versatile downstream transformations, providing a general and efficient strategy for synthesizing configurationally unstable axially chiral alkenes.

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Cite This Study

Cao et al. (2026) studied this question.

synapsesocial.com/papers/69d894ec6c1944d70ce05d0ahttps://doi.org/10.1021/acscatal.6c01105
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