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Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination and Bromination of Olefins
[Image: see text] Herein, we report the first metal-free and molecular halogen reagent-free dihomohalogenation methodology by using Selectfluor as an oxidant and tetrabutylammonium bromide/chloride salts as a halogen source. This effective strategy provides various fluorine-free halogenated products...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680025/ https://www.ncbi.nlm.nih.gov/pubmed/36129307 http://dx.doi.org/10.1021/acs.orglett.2c02627 |
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author | Dağalan, Ziya Koçak, Ramazan Daştan, Arif Nişancı, Bilal |
author_facet | Dağalan, Ziya Koçak, Ramazan Daştan, Arif Nişancı, Bilal |
author_sort | Dağalan, Ziya |
collection | PubMed |
description | [Image: see text] Herein, we report the first metal-free and molecular halogen reagent-free dihomohalogenation methodology by using Selectfluor as an oxidant and tetrabutylammonium bromide/chloride salts as a halogen source. This effective strategy provides various fluorine-free halogenated products easily in quantitative yields from alkenes, alkynes, and natural products. |
format | Online Article Text |
id | pubmed-9680025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96800252022-11-23 Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination and Bromination of Olefins Dağalan, Ziya Koçak, Ramazan Daştan, Arif Nişancı, Bilal Org Lett [Image: see text] Herein, we report the first metal-free and molecular halogen reagent-free dihomohalogenation methodology by using Selectfluor as an oxidant and tetrabutylammonium bromide/chloride salts as a halogen source. This effective strategy provides various fluorine-free halogenated products easily in quantitative yields from alkenes, alkynes, and natural products. American Chemical Society 2022-09-21 2022-11-18 /pmc/articles/PMC9680025/ /pubmed/36129307 http://dx.doi.org/10.1021/acs.orglett.2c02627 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Dağalan, Ziya Koçak, Ramazan Daştan, Arif Nişancı, Bilal Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination and Bromination of Olefins |
title | Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination
and Bromination of Olefins |
title_full | Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination
and Bromination of Olefins |
title_fullStr | Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination
and Bromination of Olefins |
title_full_unstemmed | Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination
and Bromination of Olefins |
title_short | Selectfluor and TBAX (Cl, Br) Mediated Oxidative Chlorination
and Bromination of Olefins |
title_sort | selectfluor and tbax (cl, br) mediated oxidative chlorination
and bromination of olefins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680025/ https://www.ncbi.nlm.nih.gov/pubmed/36129307 http://dx.doi.org/10.1021/acs.orglett.2c02627 |
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