Login / Signup

Determination of Enantiomeric Excess and Diastereomeric Excess via Optical Methods. Application to α-methyl-β-hydroxy-carboxylic acids.

Sarah R MoorJames R HowardBrenden T HerreraMatthew S McVeighFederico MariniAdrian T Keatinge-ClayEric V Anslyn
Published in: Organic chemistry frontiers : an international journal of organic chemistry (2023)
Characterization of chiral molecules in solution is paramount for measuring reaction success. However, techniques to distinguish between chiral molecules containing more than one stereocenter through the use of optical techniques remains a challenge. Herein, we report a techique using a series of circular dichroism spectra to train multivariate regression models that are capable of predicting the complete speciation of 3-hydroxy-2-methylbutanoic acid stereoisomers. From this, it is possible to rapidly and accurately determine the enantiomeric excess and diastereomeric excess of the solution without the need for chiral chromatography.
Keyphrases
  • capillary electrophoresis
  • high speed
  • mass spectrometry
  • high resolution
  • ionic liquid
  • liquid chromatography
  • tandem mass spectrometry
  • density functional theory
  • ms ms