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Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes

1,3‐Dithiane‐protected enones (enone dithianes) were found to undergo an intramolecular [2+2] photocycloaddition under visible‐light irradiation (λ=405 nm) in the presence of a Brønsted acid (7.5–10 mol %). Key to the success of the reaction is presumably the formation of colored thionium ions, whic...

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Autores principales: Brenninger, Christoph, Pöthig, Alexander, Bach, Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396283/
https://www.ncbi.nlm.nih.gov/pubmed/28319302
http://dx.doi.org/10.1002/anie.201700837
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author Brenninger, Christoph
Pöthig, Alexander
Bach, Thorsten
author_facet Brenninger, Christoph
Pöthig, Alexander
Bach, Thorsten
author_sort Brenninger, Christoph
collection PubMed
description 1,3‐Dithiane‐protected enones (enone dithianes) were found to undergo an intramolecular [2+2] photocycloaddition under visible‐light irradiation (λ=405 nm) in the presence of a Brønsted acid (7.5–10 mol %). Key to the success of the reaction is presumably the formation of colored thionium ions, which are intermediates of the catalytic cycle. Cyclobutanes were thus obtained in very good yields (78–90 %). It is also shown that the dithiane moiety can be reductively or oxidatively removed without affecting the photochemically constructed ring skeleton.
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spelling pubmed-53962832017-04-25 Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes Brenninger, Christoph Pöthig, Alexander Bach, Thorsten Angew Chem Int Ed Engl Communications 1,3‐Dithiane‐protected enones (enone dithianes) were found to undergo an intramolecular [2+2] photocycloaddition under visible‐light irradiation (λ=405 nm) in the presence of a Brønsted acid (7.5–10 mol %). Key to the success of the reaction is presumably the formation of colored thionium ions, which are intermediates of the catalytic cycle. Cyclobutanes were thus obtained in very good yields (78–90 %). It is also shown that the dithiane moiety can be reductively or oxidatively removed without affecting the photochemically constructed ring skeleton. John Wiley and Sons Inc. 2017-03-20 2017-04-03 /pmc/articles/PMC5396283/ /pubmed/28319302 http://dx.doi.org/10.1002/anie.201700837 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Brenninger, Christoph
Pöthig, Alexander
Bach, Thorsten
Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes
title Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes
title_full Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes
title_fullStr Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes
title_full_unstemmed Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes
title_short Brønsted Acid Catalysis in Visible‐Light‐Induced [2+2] Photocycloaddition Reactions of Enone Dithianes
title_sort brønsted acid catalysis in visible‐light‐induced [2+2] photocycloaddition reactions of enone dithianes
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396283/
https://www.ncbi.nlm.nih.gov/pubmed/28319302
http://dx.doi.org/10.1002/anie.201700837
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