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Cu-Catalyzed Direct Asymmetric Mannich Reaction of 2-Alkylazaarenes and Isatin-Derived Ketimines.

Yao-Bin ShenHui-Ling QianLei YangShun ZhouHan-Wen RaoZhen-Hua WangYong YouYan-Ping ZhangJun-Qing YinJian-Qiang ZhaoWenjing ZhangWei-Cheng Yuan
Published in: Organic letters (2024)
The first direct catalytic asymmetric Mannich reaction of 2-alkylazaarenes and ketimines was realized with a chiral Cu-bis(oxazoline) complex as the catalyst. The asymmetric addition of 2-alkylpyridines to isatin-derived ketimines proceeded smoothly to afford α,β-functionalized 2-substituted pyridines bearing 3-amino-3,3-disubstituted oxindole motifs with excellent results (≤99% yield, 99:1 dr, and 98% ee). The catalytic system was also extended to 2-alkylbenzothiazoles as nucleophiles for the asymmetric Mannich reaction of ketimines.
Keyphrases
  • ionic liquid
  • solid state
  • room temperature
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  • electron transfer
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