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Stereocontrolled generation of nucleophilic (Z)- or (E)-α-fluoroalkenylchromium reagents via carbon–fluorine bond activation: highly stereoselective synthesis of (E)- or (Z)-β-fluoroallylic alcohols

Corresponding authors
Department of Chemistry and Materials Technology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan
Fax: +81 75-724-7580
Chem. Commun., 2014,50, 1543-1545

DOI: 10.1039/C3CC47219A
Received 21 Sep 2013, Accepted 30 Nov 2013
First published online 02 Jan 2014
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