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Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene
[Image: see text] The use of vinyl electrophiles in synthesis has been hampered by the lack of access to a suitable reagent that is practical and of appropriate reactivity. In this work we introduce a vinyl thianthrenium salt as an effective vinylating reagent. The bench-stable, crystalline reagent...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391941/ https://www.ncbi.nlm.nih.gov/pubmed/34375088 http://dx.doi.org/10.1021/jacs.1c06632 |
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author | Juliá, Fabio Yan, Jiyao Paulus, Fritz Ritter, Tobias |
author_facet | Juliá, Fabio Yan, Jiyao Paulus, Fritz Ritter, Tobias |
author_sort | Juliá, Fabio |
collection | PubMed |
description | [Image: see text] The use of vinyl electrophiles in synthesis has been hampered by the lack of access to a suitable reagent that is practical and of appropriate reactivity. In this work we introduce a vinyl thianthrenium salt as an effective vinylating reagent. The bench-stable, crystalline reagent can be readily prepared from ethylene gas at atmospheric pressure in one step and is broadly useful in the annulation chemistry of (hetero)cycles, N-vinylation of heterocyclic compounds, and palladium-catalyzed cross-coupling reactions. The structural features of the thianthrene core enable a distinct synthesis and reactivity profile, unprecedented for other vinyl sulfonium derivatives. |
format | Online Article Text |
id | pubmed-8391941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83919412021-08-31 Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene Juliá, Fabio Yan, Jiyao Paulus, Fritz Ritter, Tobias J Am Chem Soc [Image: see text] The use of vinyl electrophiles in synthesis has been hampered by the lack of access to a suitable reagent that is practical and of appropriate reactivity. In this work we introduce a vinyl thianthrenium salt as an effective vinylating reagent. The bench-stable, crystalline reagent can be readily prepared from ethylene gas at atmospheric pressure in one step and is broadly useful in the annulation chemistry of (hetero)cycles, N-vinylation of heterocyclic compounds, and palladium-catalyzed cross-coupling reactions. The structural features of the thianthrene core enable a distinct synthesis and reactivity profile, unprecedented for other vinyl sulfonium derivatives. American Chemical Society 2021-08-10 2021-08-25 /pmc/articles/PMC8391941/ /pubmed/34375088 http://dx.doi.org/10.1021/jacs.1c06632 Text en © 2021 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 | Juliá, Fabio Yan, Jiyao Paulus, Fritz Ritter, Tobias Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene |
title | Vinyl
Thianthrenium Tetrafluoroborate: A Practical
and Versatile Vinylating Reagent Made from Ethylene |
title_full | Vinyl
Thianthrenium Tetrafluoroborate: A Practical
and Versatile Vinylating Reagent Made from Ethylene |
title_fullStr | Vinyl
Thianthrenium Tetrafluoroborate: A Practical
and Versatile Vinylating Reagent Made from Ethylene |
title_full_unstemmed | Vinyl
Thianthrenium Tetrafluoroborate: A Practical
and Versatile Vinylating Reagent Made from Ethylene |
title_short | Vinyl
Thianthrenium Tetrafluoroborate: A Practical
and Versatile Vinylating Reagent Made from Ethylene |
title_sort | vinyl
thianthrenium tetrafluoroborate: a practical
and versatile vinylating reagent made from ethylene |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391941/ https://www.ncbi.nlm.nih.gov/pubmed/34375088 http://dx.doi.org/10.1021/jacs.1c06632 |
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