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March 3, 2026Organic Letters0 citations

Chiral Phosphoric Acid-Catalyzed Asymmetric 4 + 2 Cycloadditions of Photogenerated o -Quinodimethanes with Vinylazaarenes

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SGShu-Wei GanYZYu ZhouYMYu-Mei Ma

Key Points

  • High yields of cyclohexyl-appended azaarenes were achieved, reaching up to 85%.
  • The reaction showcases high enantioselectivities, with up to 98% ee reported.
  • Using a chiral phosphoric acid catalyst, the study employed photogenerated o-quinodimethanes in the process.
  • Practical implications are evident, as demonstrated by successful scale-up experiments of the synthetic method.

Abstract

Chiral cyclohexyl-appended azaarenes are highly sought synthetic targets in biochemistry and medicinal chemistry. Herein we report a chiral phosphoric acid-catalyzed asymmetric 4 + 2 cycloaddition reaction between photogenerated o-quinodimethanes and alkenylazaarenes. A wide range of cyclohexyl-appended azaarenes are obtained in moderate to high yields (up to 85%) with high diastereoselectivities (up to 20:1 dr) and excellent enantioselectivities (up to 98% ee). A scale-up experiment and derivatizations of products demonstrate the practical utility of this synthetic method.

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Cite This Study

Gan et al. (2026) studied this question.

synapsesocial.com/papers/69a75c2fc6e9836116a24c72https://doi.org/10.1021/acs.orglett.5c05308
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