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February 2, 2026Organic Chemistry Frontiers0 citations

Synthesis of Chiral α-Trifluoromethyl amines via Asymmetric reaction of Trifluoromethylated Imines

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WCWei ChenWCWei ChenQYQin Yang

Key Points

  • The aim is to develop efficient synthetic methods for chiral trifluoromethyl amines due to their value as intermediates.
  • Synthesis of chiral α-trifluoromethyl amines using trifluoromethylated imines.
  • Utilization of asymmetric reaction techniques to achieve chirality.
  • Characterization of products for purity and chiral resolution.
  • Successfully synthesized various chiral α-trifluoromethyl amines.
  • Demonstrated effectiveness of the method in creating biologically active intermediates.
  • Achieved high levels of enantiomeric excess in the products.

Abstract

Chiral fluorinated amine compounds are valuable and important synthetic intermediates for the synthesis of biologically active compounds and natural products. Therefore, developing efficient synthetic methods for these compounds holds great...

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Cite This Study

Chen et al. (2026) studied this question.

synapsesocial.com/papers/6980fd3cc1c9540dea80ef93https://doi.org/10.1039/d6qo00001k
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

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  3. 3Chiral Phosphoric Acid‐Catalyzed Asymmetric Aza‐Friedel–Crafts Reaction of Indoles with Cyclic N‐Acylketimines: Enantioselective Synthesis of Trifluoromethyldihydroquinazolines2013 · 82 citations
  4. 4Enantioselective Synthesis of α‐Trifluoromethyl Arylmethylamines by Ruthenium‐Catalyzed Transfer Hydrogenation Reaction2014 · 46 citations
  5. 5Asymmetric Transfer Hydrogenation of Trifluoromethylated Imines to Chiral α‐Trifluoromethylated Amines With Alcohol as The Hydrogen Source2021 · 10 citations