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 X 10 mm, 10 (micro)m) 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.

Synthesis, chiral HPLC resolution and configuration assignment of 1-phenylglyceryl trinitrate stereomers

CHEGAEV, Konstantin;LAZZARATO, Loretta;MARABELLO, Domenica;DI STILO, Antonella;CENA, Clara;FRUTTERO, Roberta;GASCO, Alberto;
2006-01-01

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 X 10 mm, 10 (micro)m) 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
18
6
430
436
http://www3.interscience.wiley.com/journal/37532/home
absolute configuration; enantiomer separation; chiral liquid chromatography; vasodilating compound
CHEGAEV K; LAZZARATO L; TRON G.C; MARABELLO D; DI STILO A; CENA C; FRUTTERO R; GASCO A; VANTHUYNE N; ROUSSEL C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1780
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