Synthesis of α-cyano-β-fluoro-α-hydroxyesters

Article abstract of DOI:10.1080/00397919308011124

The ring opening fluorination of glycidic gem-cyanoesters was achieved by action of pyridine polyhydrofluoride at 25°C in dichloromethane. The regioselective nucleophilic substitution reaction allows the synthesis of a new class of fluorohydrins with OH,

Full text of DOI:10.1080/00397919308011124

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of α-Cyano-β-
fluoro-α-hydroxyesters
F. Ammadi a , M. M. Chaabouni a , H. Amri a & A.
Baklouti a
a Laboratoire de Chimie Organique Structurale ,
Faculté des Sciences Campus Universitaire , 1060,
Tunis, Tunisie
Published online: 23 Sep 2006.
To cite this article: F. Ammadi , M. M. Chaabouni , H. Amri & A. Baklouti (1993)
Synthesis of α-Cyano-β-fluoro-α-hydroxyesters, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 23:17,
2389-2395, DOI: 10.1080/00397919308011124
To link to this article: http://dx.doi.org/10.1080/00397919308011124
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