All-
trans biscyclohexylammonium retinylphosphate was synthesized using bis(triethylammonium)phosphate as the phosphate donor. It was shown to be pure from physico-chemical evidence including ultraviolet, infrared,
1H- and
13C-nuclear magnetic resonance and mass spectrometry. In contrast to previous reports, the synthesized product is quite stable toward alkaline hydrolysis. Direct or iodine-catalyzed photo-isomerization of the all-
trans compound can produce the corresponding 13-
cis isomer. Simultaneous quantification of
cis-trans stereoisomeric retinylphosphates was demonstrated by ion-pairing reversed-phase liquid chromatography with an isocratic mobile phase consisting of aqueous methanol and with ultraviolet detection at 300 nm. The mobile phase also contains tetrabutylammoniumphosphate as the counter-ion. The feasibility and extent of stereoisomerization of all-
trans retinylphosphate have been compared with those of carotenoidal and retinoidal polyenes.
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