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Copper-Catalyzed Asymmetric Kinugasa/Michael Addition Cascade Reactions for the Synthesis of Chiral Spiro β-Lactams.

Yunlin AoHaowen MaBinghan GanWenjing WangJiehao ZhangWei ZhouXiaoqi ZhangQian Cai
Published in: Organic letters (2024)
A mild copper-catalyzed asymmetric Kinugasa/Michael addition cascade process is developed. The reaction of α, β-unsaturated ester-tethered propiolamides with nitrones provides an efficient protocol for the construction of functionalized chiral 2,6-diazaspiro[3.4]octane-1,5-dione products in satisfactory yields and with high enantio- and diastereoselectivities.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • randomized controlled trial
  • solid state
  • quantum dots
  • mass spectrometry
  • molecularly imprinted
  • high resolution
  • solid phase extraction