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. 2020 Nov 16;16:2776–2787. doi: 10.3762/bjoc.16.228

Figure 6.

Figure 6

Separation of the enantiomers of methyl (Z)-3-hydroxy-13-octadecenoate (25) on a β-6-TBDMS hydrodex gas chromatographic phase. A) Natural extract; B) synthetic rac-25; C) synthetic (R)-25; X: methyl 3-hydroxy-11-octadecenoate; Y: methyl 3-hydroxyoctadecanoate; E: (E)-isomer of (R)-25. The enantiomer (S,E)-25 elutes together with (R,Z)-25, indicated by the broader base of this peak in B compared to C.