Synthetic cannabinoid receptor agonists were enantioseparated with Whelk-O®1 CSPs. Efficient enantioseparations were obtained under reversed-phase conditions. The developed HPLC method was compatible to MS detection. The ICCA concept was useful to appraise the enantiopurity of the studied compounds. Coupling ECD analysis to in silico simulations allowed to establish the EEO.

Varfaj, I., Protti, M., Di Michele, A., Gonzalez-Rodriguez, J., Carotti, A., Sardella, R., et al. (2024). Chromatographic enantioresolution and stereochemical characterization of synthetic cannabinoid receptor agonists with Whelk-O®1 chiral stationary phases under mass spectrometry compatible reversed-phase conditions: A study case with seized samples. ANALYTICA CHIMICA ACTA, 1317, 1-8 [10.1016/j.aca.2024.342901].

Chromatographic enantioresolution and stereochemical characterization of synthetic cannabinoid receptor agonists with Whelk-O®1 chiral stationary phases under mass spectrometry compatible reversed-phase conditions: A study case with seized samples

Protti M.
Co-primo
Membro del Collaboration Group
;
Mercolini L.
Ultimo
Membro del Collaboration Group
2024

Abstract

Synthetic cannabinoid receptor agonists were enantioseparated with Whelk-O®1 CSPs. Efficient enantioseparations were obtained under reversed-phase conditions. The developed HPLC method was compatible to MS detection. The ICCA concept was useful to appraise the enantiopurity of the studied compounds. Coupling ECD analysis to in silico simulations allowed to establish the EEO.
2024
Varfaj, I., Protti, M., Di Michele, A., Gonzalez-Rodriguez, J., Carotti, A., Sardella, R., et al. (2024). Chromatographic enantioresolution and stereochemical characterization of synthetic cannabinoid receptor agonists with Whelk-O®1 chiral stationary phases under mass spectrometry compatible reversed-phase conditions: A study case with seized samples. ANALYTICA CHIMICA ACTA, 1317, 1-8 [10.1016/j.aca.2024.342901].
Varfaj, I.; Protti, M.; Di Michele, A.; Gonzalez-Rodriguez, J.; Carotti, A.; Sardella, R.; Mercolini, L.
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