Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence

Remete, Attila Márió; Nonn, Melinda; Fustero, Santos; Haukka, Matti; Fülöp, Ferenc; Kiss, Loránd

doi:10.3762/bjoc.13.233

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Remete, A. M., Nonn, M., Fustero, S., Haukka, M., Fülöp, F., & Kiss, L. (2017). Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence. Beilstein Journal of Organic Chemistry, 13, 2364-2371. https://doi.org/10.3762/bjoc.13.233

Julkaistu sarjassa

Beilstein Journal of Organic Chemistry

Tekijät

Remete, Attila Márió |

Nonn, Melinda |

Fustero, Santos |

Haukka, Matti |

Fülöp, Ferenc |

Kiss, Loránd

Päivämäärä

2017

Oppiaine

Epäorgaaninen ja analyyttinen kemia Inorganic and Analytical Chemistry

Tekijänoikeudet

A study exploring the chemical behavior of some dihydroxylated β-amino ester stereo- and regioisomers, derived from unsaturated cyclic β-amino acids is described. The nucleophilic fluorinations involving hydroxy–fluorine exchange of some highly functionalized alicyclic diol derivatives have been carried out in view of selective fluorination, investigating substrate dependence, neighboring group assistance and chemodifferentiation.

Julkaisija

Beilstein-Institut

ISSN Hae Julkaisufoorumista

2195-951X

Lisenssi

© 2017 Remete et al.; licensee Beilstein-Institut. This is an open access article distributed under the terms of a Creative Commons License.

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