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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...

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Autores principales: Remete, Attila Márió, Novák, Tamás T, Nonn, Melinda, Haukka, Matti, Fülöp, Ferenc, Kiss, Loránd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
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.
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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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