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Highly Enantioselective Extraction of Phenylglycine by a Chiral Macrocyclic Receptor Based on Supramolecular Interactions.

María G TurielJosé J Garrido-GonzálezLuis SimónFrancisca SanzAnna M LithgowJoaquín R MoránAngel L Fuentes de ArribaVictoria Alcázar Montero
Published in: Organic letters (2020)
Using supramolecular interactions, a novel macrocyclic receptor is able to selectively extract zwitterionic phenylglycine from neutral aqueous solutions into chloroform with up to 91.8% ee. Modeling studies, nuclear magnetic resonance experiments, and X-ray diffraction analysis were carried out to explain the high enantioselectivity observed.
Keyphrases
  • magnetic resonance
  • high resolution
  • energy transfer
  • binding protein
  • computed tomography
  • mass spectrometry
  • case control
  • dual energy