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P / N -Heteroleptic Cu(I)-Photosensitizer-Catalyzed [3 + 2] Regiospecific Annulation of Aminocyclopropanes and Functionalized Alkynes.

Lailin ChenYa LiMingfeng HanYun PengXiahe ChenSiwei XiangHong GaoTianhao LuShu-Ping LuoBingwei ZhouHua-Yue WuYun-Fang YangYunkui Liu
Published in: The Journal of organic chemistry (2022)
We report here a regiospecific [3 + 2] annulation between aminocyclopropanes and various functionalized alkynes enabled by a P / N -heteroleptic Cu(I) photosensitizer under photoredox catalysis conditions. Thus, a divergent construction of 3-aminocyclopentene derivatives including methylsulfonyl-, arylsulfonyl-, chloro-, ester-, and trifluoromethyl-functionalized aminocyclopentenes could be achieved with advantages of high regioselectivity, broad substrate compatibility, and mild and environmentally benign reaction conditions.
Keyphrases
  • high resolution
  • photodynamic therapy
  • quantum dots
  • mass spectrometry
  • molecularly imprinted
  • visible light
  • aqueous solution
  • metal organic framework
  • amino acid