Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence
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
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Beilstein Journal of Organic ChemistryDate
2017Copyright
© 2017 Remete et al.; licensee Beilstein-Institut. This is an open access article distributed under the terms of a Creative Commons License.
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.
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Except where otherwise noted, this item's license is described as © 2017 Remete et al.; licensee Beilstein-Institut. This is an open access article distributed under the terms of a Creative Commons License.