Enatiomeric separation of branched fatty acids after conversion with trans-2-(2,3-Anthracenedicarboximido)cyclohexanol, a highly sensitive chiral fluorescent conversion reagent

Article abstract of DOI:10.1271/bbb.63.1209

(1R,2R)-2-(2,3-Anthracenedicarboximido)cyclohexanol was synthesized as a highly sensitive chiral fluorescent conversion reagent. The diastereomeric derivatives of chiral branched fatty acids that had methyl ethyl chirality from the 2 to 12 position were separated into 2 peaks by reversed-phase HPLC and detected at the 10^-15 mole level by fluorometry.