Issue 2, 2000
From the journal:

Chemical Communications

Highly enantioselective propargylic monofluorination established by carbon-13 and fluorine-19

Valérie Madiot,a   Philippe Lesot,*b   Danielle Grée,a   Jacques Courtieub  and  René Gree*a  

* Corresponding authors

a Laboratoire de Synthèses et Activations de Biomolécules CNRS ESA 6052, ENSCR, Avenue du Général Leclerc, Rennes Beaulieu, France.
E-mail: gree@ensc-rennes.fr

b Laboratoire de Chimie Structurale Organique, CNRS ESA 8074, ICMO, Bât 410, Université de Paris-Sud, Orsay, France.
E-mail: philesot@icmo.u-psud.fr

Abstract

Carbon-13 and fluorine-19 NMR experiments in a chiral polypeptide liquid crystalline solvent (PBLG) are used to establish enantioselective propargylic monofluorination.

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Article information

DOI
https://doi.org/10.1039/A909012F
Article type
Communication
Submitted
12 Nov 1999
Accepted
06 Dec 1999
First published
17 Jan 2000

Chem. Commun., 2000, 169-170

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

V. Madiot, P. Lesot, D. Grée, J. Courtieu and R. Gree, Chem. Commun., 2000, 169 DOI: 10.1039/A909012F

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