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Published on: April 15, 2013
Enatiomeric Separation of Branched Fatty Acids after Conversion with
1a Division of Applied Life Science, Graduate School of Agricultural Science, Tohoku University.
Abstract:
(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.
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