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Synthesis of novel fluorinated building blocks via halofluorination and related reactions
A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based on electrophilic activation through halonium ions o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590628/ https://www.ncbi.nlm.nih.gov/pubmed/33133288 http://dx.doi.org/10.3762/bjoc.16.208 |
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author | Remete, Attila Márió Novák, Tamás T Nonn, Melinda Haukka, Matti Fülöp, Ferenc Kiss, Loránd |
author_facet | Remete, Attila Márió Novák, Tamás T Nonn, Melinda Haukka, Matti Fülöp, Ferenc Kiss, Loránd |
author_sort | Remete, Attila Márió |
collection | PubMed |
description | A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based on electrophilic activation through halonium ions of the ring olefin bonds, followed by nucleophilic fluorination with Deoxo-Fluor(®). The fluorine-containing products thus obtained were subjected to elimination reactions, yielding various fluorine-containing small-molecular entities. |
format | Online Article Text |
id | pubmed-7590628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-75906282020-10-30 Synthesis of novel fluorinated building blocks via halofluorination and related reactions Remete, Attila Márió Novák, Tamás T Nonn, Melinda Haukka, Matti Fülöp, Ferenc Kiss, Loránd Beilstein J Org Chem Full Research Paper A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based on electrophilic activation through halonium ions of the ring olefin bonds, followed by nucleophilic fluorination with Deoxo-Fluor(®). The fluorine-containing products thus obtained were subjected to elimination reactions, yielding various fluorine-containing small-molecular entities. Beilstein-Institut 2020-10-16 /pmc/articles/PMC7590628/ /pubmed/33133288 http://dx.doi.org/10.3762/bjoc.16.208 Text en Copyright © 2020, 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). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. 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 Novák, Tamás T Nonn, Melinda Haukka, Matti Fülöp, Ferenc Kiss, Loránd Synthesis of novel fluorinated building blocks via halofluorination and related reactions |
title | Synthesis of novel fluorinated building blocks via halofluorination and related reactions |
title_full | Synthesis of novel fluorinated building blocks via halofluorination and related reactions |
title_fullStr | Synthesis of novel fluorinated building blocks via halofluorination and related reactions |
title_full_unstemmed | Synthesis of novel fluorinated building blocks via halofluorination and related reactions |
title_short | Synthesis of novel fluorinated building blocks via halofluorination and related reactions |
title_sort | synthesis of novel fluorinated building blocks via halofluorination and related reactions |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590628/ https://www.ncbi.nlm.nih.gov/pubmed/33133288 http://dx.doi.org/10.3762/bjoc.16.208 |
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