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Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence
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 car...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687045/ https://www.ncbi.nlm.nih.gov/pubmed/29181116 http://dx.doi.org/10.3762/bjoc.13.233 |
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author | Remete, Attila Márió Nonn, Melinda Fustero, Santos Haukka, Matti Fülöp, Ferenc Kiss, Loránd |
author_facet | Remete, Attila Márió Nonn, Melinda Fustero, Santos Haukka, Matti Fülöp, Ferenc Kiss, Loránd |
author_sort | Remete, Attila Márió |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5687045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-56870452017-11-27 Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence Remete, Attila Márió Nonn, Melinda Fustero, Santos Haukka, Matti Fülöp, Ferenc Kiss, Loránd Beilstein J Org Chem Full Research Paper 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. Beilstein-Institut 2017-11-06 /pmc/articles/PMC5687045/ /pubmed/29181116 http://dx.doi.org/10.3762/bjoc.13.233 Text en Copyright © 2017, Remete et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Remete, Attila Márió Nonn, Melinda Fustero, Santos Haukka, Matti Fülöp, Ferenc Kiss, Loránd Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
title | Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
title_full | Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
title_fullStr | Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
title_full_unstemmed | Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
title_short | Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
title_sort | fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687045/ https://www.ncbi.nlm.nih.gov/pubmed/29181116 http://dx.doi.org/10.3762/bjoc.13.233 |
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