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Electroreductive Ring-Opening Carboxylation of 1,3-Oxazolidin-2-ones with CO 2 for Accessing β-Amino Acids.

Li TaoXiao-Fei LiuBai-Hao RenHe WangHui-Qin SunKe ZhangYong-Qiang TengWei-Min RenXiao-Bing LuWen-Zhen Zhang
Published in: Organic letters (2024)
Electrocarboxylation of the C(sp 3 )-O bond in 1,3-oxazolidin-2-ones with CO 2 to achieve β-amino acids is developed. The C-O bond in substrates can be selectively cleaved via the single electron transfer on the surface of a cathode or through a CO 2 •   - intermediate under additive-free conditions. A great diversity of β-amino acids can be obtained in a moderate to excellent yield and readily converted to various biologically active compounds.
Keyphrases
  • amino acid
  • electron transfer
  • high intensity
  • transition metal