Highly enantioselective propargylic monofluorination established by carbon-13 and fluorine-19 NMR in chiral liquid crystals

Abstract : Carbon-13 and fluorine-19 NMR experiments in a chiral polypeptide liquid crystalline solvent (PBLG) are used to establish enantioselective propargylic monofluorination.
Document type :
Journal articles
Complete list of metadatas

https://hal.archives-ouvertes.fr/hal-02309109
Contributor : Philippe Lesot <>
Submitted on : Wednesday, October 9, 2019 - 8:18:00 AM
Last modification on : Tuesday, October 29, 2019 - 7:14:03 PM

Identifiers

Citation

Valérie Madiot, Philippe Lesot, Danielle Gree, Jacques Courtieu, René Grée. Highly enantioselective propargylic monofluorination established by carbon-13 and fluorine-19 NMR in chiral liquid crystals. Chemical Communications, Royal Society of Chemistry, 2000, pp.169-170. ⟨10.1039/A909012F⟩. ⟨hal-02309109⟩

Share

Metrics

Record views

22