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Highly efficient one-step microwave-assisted synthesis of structurally diverse bis-substituted α-amino acid derived diimides.

Marcin KonopkaGrzegorz MarkiewiczArtur R Stefankiewicz
Published in: RSC advances (2018)
We report herein a facile and widely applicable microwave-assisted protocol for the synthesis of symmetrical diimides based on three structurally distinct aromatic dianhydrides: pyromellitic (PMA), biphenyl-tetracarboxylic acid (BPDA) and benzophenone-tetracarboxylic (BTDA) and five natural amino acids (Phe, Tyr, Ile, Lys, Cys). Fifteen symmetrical diimides with different structural characteristics containing a variety of functional groups can be produced with high yields and on a large scale.
Keyphrases
  • amino acid
  • highly efficient
  • randomized controlled trial
  • molecular docking
  • ionic liquid
  • gold nanoparticles
  • molecular dynamics simulations