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A One-Pot Iodo-Cyclization/Transition Metal-Catalyzed Cross-Coupling Sequence: Synthesis of Substituted Oxazolidin-2-ones from N-Boc-allylamines.

Pauline Chaumont-OliveJanine Cossy
Published in: Organic letters (2020)
A one-pot iodo-cyclization/transition metal-catalyzed cross-coupling sequence is reported to access various C5-functionalized oxazolidin-2-ones from unsaturated N-Boc-allylamines. Depending on the Grignard reagents used for the cross-coupling, e.g., aryl- or cyclopropylmagnesium bromide, a cobalt or copper catalyst has to be used to obtain the functionalized oxazolidin-2-ones in good yields.
Keyphrases
  • transition metal
  • room temperature
  • quantum dots
  • reduced graphene oxide
  • ionic liquid
  • molecularly imprinted
  • metal organic framework
  • molecular docking
  • amino acid
  • highly efficient
  • carbon dioxide
  • mass spectrometry