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EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts

Despite their long-known photochemical properties and their industrial value, the use of nitroarenes as a productive photochemical handle in organic synthesis has remained relatively unexplored. More specifically, the photochemical formation of nitrogen-sulfur bonds from nitroarenes remains to be de...

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Autores principales: Lasso, Juan D., Castillo-Pazos, Durbis J., Sim, Malcolm, Barroso-Flores, Joaquín, Li, Chao-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847664/
https://www.ncbi.nlm.nih.gov/pubmed/36741536
http://dx.doi.org/10.1039/d2sc06087f
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author Lasso, Juan D.
Castillo-Pazos, Durbis J.
Sim, Malcolm
Barroso-Flores, Joaquín
Li, Chao-Jun
author_facet Lasso, Juan D.
Castillo-Pazos, Durbis J.
Sim, Malcolm
Barroso-Flores, Joaquín
Li, Chao-Jun
author_sort Lasso, Juan D.
collection PubMed
description Despite their long-known photochemical properties and their industrial value, the use of nitroarenes as a productive photochemical handle in organic synthesis has remained relatively unexplored. More specifically, the photochemical formation of nitrogen-sulfur bonds from nitroarenes remains to be demonstrated. Herein, we report the design and application of a sulfinate–nitroarene electron donor–acceptor (EDA) complex and its subsequent use in the first light mediated catalyst-free synthesis of N-hydroxy-sulfonamides. The presence of the EDA was assessed spectroscopically and studied via DFT and TD-DFT calculations. A total of 32 examples including both electron withdrawing and electron donating groups were synthesized under our oxygen- and water-tolerant conditions.
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spelling pubmed-98476642023-02-03 EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts Lasso, Juan D. Castillo-Pazos, Durbis J. Sim, Malcolm Barroso-Flores, Joaquín Li, Chao-Jun Chem Sci Chemistry Despite their long-known photochemical properties and their industrial value, the use of nitroarenes as a productive photochemical handle in organic synthesis has remained relatively unexplored. More specifically, the photochemical formation of nitrogen-sulfur bonds from nitroarenes remains to be demonstrated. Herein, we report the design and application of a sulfinate–nitroarene electron donor–acceptor (EDA) complex and its subsequent use in the first light mediated catalyst-free synthesis of N-hydroxy-sulfonamides. The presence of the EDA was assessed spectroscopically and studied via DFT and TD-DFT calculations. A total of 32 examples including both electron withdrawing and electron donating groups were synthesized under our oxygen- and water-tolerant conditions. The Royal Society of Chemistry 2022-12-15 /pmc/articles/PMC9847664/ /pubmed/36741536 http://dx.doi.org/10.1039/d2sc06087f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Lasso, Juan D.
Castillo-Pazos, Durbis J.
Sim, Malcolm
Barroso-Flores, Joaquín
Li, Chao-Jun
EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts
title EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts
title_full EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts
title_fullStr EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts
title_full_unstemmed EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts
title_short EDA mediated S–N bond coupling of nitroarenes and sodium sulfinate salts
title_sort eda mediated s–n bond coupling of nitroarenes and sodium sulfinate salts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847664/
https://www.ncbi.nlm.nih.gov/pubmed/36741536
http://dx.doi.org/10.1039/d2sc06087f
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