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

Valérie Madiot 1 Philippe Lesot 2, 3, * Danielle Gree 1 Jacques Courtieu 2 René Grée 1, 3, *
* Corresponding author
1 ISCR - Institut des Sciences Chimiques de Rennes
2 ICMMO - Institut de Chimie Moléculaire et des Matériaux d'Orsay
3 CNRS - Centre National de la Recherche Scientifique
Abstract : Carbon-13 and fluorine-19 NMR experiments in a chiral polypeptide liquid crystalline solvent (PBLG) are used to establish enantioselective propargylic monofluorination.
Keywords : polypeptide PBLG Enantioselectivity Monofluoration Carbon-13 NMR chiral liquid crystalline solvent Fluorine-19
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

Collections

UNIV-RENNES1 | CNRS | INC-CNRS | ISCR | UNIV-RENNES | INSA-GROUPE | UR1-UFR-SPM

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⟩

Export

BibTeX TEI DC DCterms EndNote

Share

Metrics

Record views

22

Contact

Informations

CCSD