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Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst for SOMOphilic Alkynylation
[Image: see text] A versatile approach for the alkynylation of a variety of aliphatic hydrogen donors, including alkanes, is reported. We used tetrabutylammonium decatungstate as photocatalyst to generate organoradicals from C–H/Si–H bonds via hydrogen atom transfer. The latter intermediates underwe...
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/PMC8041368/ https://www.ncbi.nlm.nih.gov/pubmed/33656899 http://dx.doi.org/10.1021/acs.orglett.1c00381 |
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author | Capaldo, Luca Ravelli, Davide |
author_facet | Capaldo, Luca Ravelli, Davide |
author_sort | Capaldo, Luca |
collection | PubMed |
description | [Image: see text] A versatile approach for the alkynylation of a variety of aliphatic hydrogen donors, including alkanes, is reported. We used tetrabutylammonium decatungstate as photocatalyst to generate organoradicals from C–H/Si–H bonds via hydrogen atom transfer. The latter intermediates underwent SOMOphilic alkynylation by methanesulfonyl alkynes to afford internal alkynes upon loss of a sulfonyl radical. The effect of different radicofugal groups on the reaction outcome was evaluated and rationalized via a combined experimental and computational approach. |
format | Online Article Text |
id | pubmed-8041368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80413682021-04-13 Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst for SOMOphilic Alkynylation Capaldo, Luca Ravelli, Davide Org Lett [Image: see text] A versatile approach for the alkynylation of a variety of aliphatic hydrogen donors, including alkanes, is reported. We used tetrabutylammonium decatungstate as photocatalyst to generate organoradicals from C–H/Si–H bonds via hydrogen atom transfer. The latter intermediates underwent SOMOphilic alkynylation by methanesulfonyl alkynes to afford internal alkynes upon loss of a sulfonyl radical. The effect of different radicofugal groups on the reaction outcome was evaluated and rationalized via a combined experimental and computational approach. American Chemical Society 2021-03-03 2021-03-19 /pmc/articles/PMC8041368/ /pubmed/33656899 http://dx.doi.org/10.1021/acs.orglett.1c00381 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Capaldo, Luca Ravelli, Davide Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst for SOMOphilic Alkynylation |
title | Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst
for SOMOphilic Alkynylation |
title_full | Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst
for SOMOphilic Alkynylation |
title_fullStr | Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst
for SOMOphilic Alkynylation |
title_full_unstemmed | Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst
for SOMOphilic Alkynylation |
title_short | Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst
for SOMOphilic Alkynylation |
title_sort | decatungstate as direct hydrogen atom transfer photocatalyst
for somophilic alkynylation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041368/ https://www.ncbi.nlm.nih.gov/pubmed/33656899 http://dx.doi.org/10.1021/acs.orglett.1c00381 |
work_keys_str_mv | AT capaldoluca decatungstateasdirecthydrogenatomtransferphotocatalystforsomophilicalkynylation AT ravellidavide decatungstateasdirecthydrogenatomtransferphotocatalystforsomophilicalkynylation |