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Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light
A novel and sustainable procedure was developed for the synthesis of 3-selenylindoles employing diorganyl diselenides and indoles or electron-rich arenes as starting materials. Visible blue light was used to promote the reaction without employing transition metal complexes or organic photocatalysts...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067025/ https://www.ncbi.nlm.nih.gov/pubmed/35519497 http://dx.doi.org/10.1039/c9ra03642c |
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author | Lemir, Ignacio D. Castro-Godoy, Willber D. Heredia, Adrián A. Schmidt, Luciana C. Argüello, Juan E. |
author_facet | Lemir, Ignacio D. Castro-Godoy, Willber D. Heredia, Adrián A. Schmidt, Luciana C. Argüello, Juan E. |
author_sort | Lemir, Ignacio D. |
collection | PubMed |
description | A novel and sustainable procedure was developed for the synthesis of 3-selenylindoles employing diorganyl diselenides and indoles or electron-rich arenes as starting materials. Visible blue light was used to promote the reaction without employing transition metal complexes or organic photocatalysts as sensitizers. Additives such as strong oxidants or bases were not required. Moreover, ethanol was employed as a benign solvent under mild reaction conditions. Through this easy and eco-friendly approach, several 3-selenylindoles and a number of asymmetric diarylselenides were obtained in good to excellent isolated yields. |
format | Online Article Text |
id | pubmed-9067025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90670252022-05-04 Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light Lemir, Ignacio D. Castro-Godoy, Willber D. Heredia, Adrián A. Schmidt, Luciana C. Argüello, Juan E. RSC Adv Chemistry A novel and sustainable procedure was developed for the synthesis of 3-selenylindoles employing diorganyl diselenides and indoles or electron-rich arenes as starting materials. Visible blue light was used to promote the reaction without employing transition metal complexes or organic photocatalysts as sensitizers. Additives such as strong oxidants or bases were not required. Moreover, ethanol was employed as a benign solvent under mild reaction conditions. Through this easy and eco-friendly approach, several 3-selenylindoles and a number of asymmetric diarylselenides were obtained in good to excellent isolated yields. The Royal Society of Chemistry 2019-07-23 /pmc/articles/PMC9067025/ /pubmed/35519497 http://dx.doi.org/10.1039/c9ra03642c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Lemir, Ignacio D. Castro-Godoy, Willber D. Heredia, Adrián A. Schmidt, Luciana C. Argüello, Juan E. Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
title | Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
title_full | Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
title_fullStr | Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
title_full_unstemmed | Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
title_short | Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
title_sort | metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067025/ https://www.ncbi.nlm.nih.gov/pubmed/35519497 http://dx.doi.org/10.1039/c9ra03642c |
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