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Axially Chiral Trifluoromethylbenzimidazolylbenzoic Acid: A Chiral Derivatizing Agent for α-Chiral Primary Amines and Secondary Alcohols To Determine the Absolute Configuration.

Michal KriegelsteinDavid ProfousAntonín LyčkaZdeněk TrávníčekAdam PřibylkaTereza VolnáSandra BenickáPetr Cankař
Published in: The Journal of organic chemistry (2019)
Racemic 2-(2-trifluoromethyl)-1H-benzo[d]imidazol-1-yl)benzoic acid (TBBA) was synthesized in three steps from 1-fluoro-2-nitrobenzene. Target (P)- and (M)-TBBA atropisomers were stable with a racemization barrier above 30 kcal/mol. As a chiral derivatizing agent, TBBA showed much higher differences in chemical shifts (ΔδPM) than the conventional Mosher's acid.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • mass spectrometry
  • heavy metals
  • polycyclic aromatic hydrocarbons
  • pet ct