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

  • Konstantin Chegaev
  • , Loretta Lazzarato
  • , Gian Cesare Tron
  • , Domenica Marabello
  • , Antonella Di Stilo
  • , Clara Cena
  • , Roberta Fruttero
  • , Alberto Gasco
  • , Nicolas Vanthuyne
  • , Christian Roussel

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)430-436
Number of pages7
JournalChirality
Volume18
Issue number6
DOIs
Publication statusPublished - 2006

Keywords

  • Absolute configuration
  • Chiral liquid chromatography
  • Enantiomer separation
  • Vasodilating compound

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