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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...

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Autores principales: Juliá, Fabio, Yan, Jiyao, Paulus, Fritz, Ritter, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
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.
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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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