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Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes
A visible‐light organophotocatalytic [2+2] cycloaddition of electron‐deficient styrenes is described. Photocatalytic [2+2] cycloadditions are typically performed with electron‐rich styrene derivatives or α,β‐unsaturated carbonyl compounds, and with transition‐metal‐based catalysts. We have discovere...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100360/ https://www.ncbi.nlm.nih.gov/pubmed/36282627 http://dx.doi.org/10.1002/chem.202202373 |
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author | Golfmann, Maxim Glagow, Louis Giakoumidakis, Antonios Golz, Christopher Walker, Johannes C. L. |
author_facet | Golfmann, Maxim Glagow, Louis Giakoumidakis, Antonios Golz, Christopher Walker, Johannes C. L. |
author_sort | Golfmann, Maxim |
collection | PubMed |
description | A visible‐light organophotocatalytic [2+2] cycloaddition of electron‐deficient styrenes is described. Photocatalytic [2+2] cycloadditions are typically performed with electron‐rich styrene derivatives or α,β‐unsaturated carbonyl compounds, and with transition‐metal‐based catalysts. We have discovered that an organic cyanoarene photocatalyst is able to deliver high‐value cyclobutane products bearing electron‐deficient aryl substituents in good yields. A range of electron‐deficient substituents are tolerated, and both homodimerisations and intramolecular [2+2] cycloadditions to fused bicyclic systems are available by using this methodology. |
format | Online Article Text |
id | pubmed-10100360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101003602023-04-14 Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes Golfmann, Maxim Glagow, Louis Giakoumidakis, Antonios Golz, Christopher Walker, Johannes C. L. Chemistry Research Articles A visible‐light organophotocatalytic [2+2] cycloaddition of electron‐deficient styrenes is described. Photocatalytic [2+2] cycloadditions are typically performed with electron‐rich styrene derivatives or α,β‐unsaturated carbonyl compounds, and with transition‐metal‐based catalysts. We have discovered that an organic cyanoarene photocatalyst is able to deliver high‐value cyclobutane products bearing electron‐deficient aryl substituents in good yields. A range of electron‐deficient substituents are tolerated, and both homodimerisations and intramolecular [2+2] cycloadditions to fused bicyclic systems are available by using this methodology. John Wiley and Sons Inc. 2022-11-27 2023-01-12 /pmc/articles/PMC10100360/ /pubmed/36282627 http://dx.doi.org/10.1002/chem.202202373 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Golfmann, Maxim Glagow, Louis Giakoumidakis, Antonios Golz, Christopher Walker, Johannes C. L. Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes |
title | Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes
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title_full | Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes
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title_fullStr | Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes
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title_full_unstemmed | Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes
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title_short | Organophotocatalytic [2+2] Cycloaddition of Electron‐Deficient Styrenes
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title_sort | organophotocatalytic [2+2] cycloaddition of electron‐deficient styrenes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100360/ https://www.ncbi.nlm.nih.gov/pubmed/36282627 http://dx.doi.org/10.1002/chem.202202373 |
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