Abstract
Studies of the perturbing effect of chiral solvating agents (CSAs) namely the fluoroalcohols 5a and 5b upon the NMR spectra of chiral Δ2‐thiazolines 1 presenting interesting insecticidal properties demonstrated the ability of these CSAs to afford diastereomeric solvates from these substrates providing their enantiomeric discrimination. Thus, for five of the six tested Δ2‐thiazolines 1A and 1B there is at least one possibility to proceed to their enantiomeric discrimination either by 1H or 19F NMR using mostly 5b as CSA.
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