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

Authors
Madiot, V Lesot, P Gree, D Courtieu, J Gree, R
Citation
V. Madiot et al., Highly enantioselective propargylic monofluorination established by carbon-13 and fluorine-19 NMR in chiral liquid crystals, CHEM COMMUN, (2), 2000, pp. 169-170
Citations number
20
Categorie Soggetti
Chemistry
Journal title
CHEMICAL COMMUNICATIONS
ISSN journal
13597345 → ACNP
Issue
2
Year of publication
2000
Pages
169 - 170
Database
ISI
SICI code
1359-7345(2000):2<169:HEPMEB>2.0.ZU;2-C
Abstract
Carbon-13 and fluorine-19 NMR experiments in a chiral polypeptide liquid cr ystalline solvent (PBLG) are used to establish enantioselective propargylic monofluorination.