4.5 Review

Self-Disproportionation of Enantiomers of Chiral, Non-Racemic Fluoroorganic Compounds: Role of Fluorine as Enabling Element

期刊

SYNTHESIS-STUTTGART
卷 45, 期 2, 页码 141-152

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0032-1316812

关键词

fluorine; fluorine compounds; optical purification; chiral recognition; chromatography; physicochemical phase transitions; amino acids; amines; hydroxy acids

资金

  1. IKERBASQUE, Basque Foundation for Science

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This review discusses all available literature on the self-disproportionation of enantiomers (SDE) of fluorine-containing compounds, resulting in a separation of racemic form from the excess enantiomer. Included are examples of the SDE via distillation, sublimation and achiral chromatography. The role of fluorine on the magnitude and preparative efficiency of the SDE, as a new, nonconventional method for optical purifications, is emphasized and critically discussed. 1 Introduction 2 General Aspects of Fluorine Influence on the Self-Disproportionation of Enantiomers 3 Self-Disproportionation of Enantiomers via Distillation 4 Self-Disproportionation of Enantiomers via Sublimation 5 Self-Disproportionation of Enantiomers via Achiral Chromatography 6 Conclusions

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