Abstract
As an introductory study of in vitro vasodilating activity, the access to the four stereomers of 1-phenylglyceryl trinitrate is described using achiral and chiral chromatography. For semi-preparative separation of the enantiomers, a Chiralcel OD (250 × 10 mm, 10 μm) was used. Catalytic reduction leading to the corresponding stereomers of 1-phenylglycerol allowed absolute configuration assignments. The same methods were used for the separation and configuration assignment of the enantiomers of 3-phenylpropane-1,2-diyl dinitrate. © 2006 Wiley-Liss, Inc.
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Chegaev, K., Lazzarato, L., Tron, G. C., Marabello, D., Di Stilo, A., Cena, C., … Roussel, C. (2006). Synthesis, chiral HPLC resolution and configuration assignment of 1-phenylglyceryl trinitrate stereomers. Chirality, 18(6), 430–436. https://doi.org/10.1002/chir.20278
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