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Catalytic Asymmetric Construction of β-Azido Amides and Esters via Haloazidation.

Pengfei ZhouXiao-Hua LiuWangbin WuChaoran XuXiaoming Feng
Published in: Organic letters (2019)
A catalytic regio- and enantioselective haloazidation reaction with a chiral iron(II) complex catalyst under mild reaction conditions was reported. By this approach, the stereoselective α-halo-β-azido difunctionalization of both α,β-unsaturated amides and α,β-unsaturated esters was achieved. This method enabled the construction of a broad spectrum of valuable functionalized amides and esters, including enantiomerically enriched β-azido amides, aziridine amides, α-amino amide derivatives, β-triazole amides, functionalized peptide derivatives, and α-halo-β-azido-substituted esters.
Keyphrases
  • quantum dots
  • mass spectrometry
  • capillary electrophoresis