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March 28, 2026Chemistry - A European Journal2 citations

General, Catalytic Asymmetric Reductive Alkynylation of Tertiary Aliphatic and Aromatic Amides by Cooperative Catalysis With Iridium/Copper/Carreira's PINAP

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FXFang-Fang XuJCJin‐Quan ChenPHPei‐Qiang Huang

Key Points

  • The aim is to develop a general protocol for the asymmetric reductive alkynylation of both aromatic and aliphatic tertiary amides.
  • Utilized Vaska's complex/CuI/Carreira's (R,P)-PINAP as the catalytic system.
  • Employed 1,1,3,3-tetramethyl-disiloxane (TMDS) as the hydrosilylation reagent.
  • Extended methodology to various functionalized alkynes.
  • Successfully achieved good reagent economy and excellent asymmetric induction.
  • Extended method applicability to tertiary aromatic amides.
  • Highlighted broad functional group tolerance and chemoselectivity in reactions.

Abstract

Chiral propargylamines are a class of versatile building blocks in organic synthesis. Despite the recent breakthroughs on the catalytic asymmetric reductive alkynylation of amides to access propargylamines, a general protocol amenable to both aromatic and aliphatic tertiary amides remains elusive. Herein, we report that our recently developed methodology for the catalytic asymmetric reductive alkynylation of tertiary aliphatic amides can be extended to tertiary aromatic amides. Employing Vaska's complex/CuI/Carreira's (R,P)-PINAP ligand as the catalytic system and 1,1,3,3-tetramethyl-disiloxane (TMDS) as the hydrosilylation reagent, the method highlights good reagent economy and/ or excellent asymmetric induction as compared to the known ones. Moreover, the reductive alkynylation of tertiary aliphatic amides has been extended to a series of functionalized alkynes. It is expectable that the versatility, excellent functional group tolerance, and chemoselectivity of the method lay the foundation for diverse applications in organic synthesis and medicinal chemistry.

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Cite This Study

Xu et al. (2026) studied this question.

synapsesocial.com/papers/69c771198bbfbc51511e102bhttps://doi.org/10.1002/chem.70919
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