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Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles

The synthetic application of (hetero)aryl radicals in organic synthesis has been known since the last century. However, their applicability has significantly suffered from ineffective generation protocols. Herein, we present a visible-light-induced transition metal-free (hetero)aryl radical generati...

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Autores principales: Majhi, Jadab, Granados, Albert, Matsuo, Bianca, Ciccone, Vittorio, Dhungana, Roshan K., Sharique, Mohammed, Molander, Gary A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890556/
https://www.ncbi.nlm.nih.gov/pubmed/36755706
http://dx.doi.org/10.1039/d2sc05918e
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author Majhi, Jadab
Granados, Albert
Matsuo, Bianca
Ciccone, Vittorio
Dhungana, Roshan K.
Sharique, Mohammed
Molander, Gary A.
author_facet Majhi, Jadab
Granados, Albert
Matsuo, Bianca
Ciccone, Vittorio
Dhungana, Roshan K.
Sharique, Mohammed
Molander, Gary A.
author_sort Majhi, Jadab
collection PubMed
description The synthetic application of (hetero)aryl radicals in organic synthesis has been known since the last century. However, their applicability has significantly suffered from ineffective generation protocols. Herein, we present a visible-light-induced transition metal-free (hetero)aryl radical generation from readily available (hetero)aryl halides for the synthesis of 3,3′-disubstituted oxindoles. This transformation is amenable to a wide range of (hetero)aryl halides as well as several easily accessible acrylamides, and it is also scalable to multigram synthesis. Finally, the versatility of the oxindole products is demonstrated through their conversion to a variety of useful intermediates applicable to target-directed synthesis.
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spelling pubmed-98905562023-02-07 Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles Majhi, Jadab Granados, Albert Matsuo, Bianca Ciccone, Vittorio Dhungana, Roshan K. Sharique, Mohammed Molander, Gary A. Chem Sci Chemistry The synthetic application of (hetero)aryl radicals in organic synthesis has been known since the last century. However, their applicability has significantly suffered from ineffective generation protocols. Herein, we present a visible-light-induced transition metal-free (hetero)aryl radical generation from readily available (hetero)aryl halides for the synthesis of 3,3′-disubstituted oxindoles. This transformation is amenable to a wide range of (hetero)aryl halides as well as several easily accessible acrylamides, and it is also scalable to multigram synthesis. Finally, the versatility of the oxindole products is demonstrated through their conversion to a variety of useful intermediates applicable to target-directed synthesis. The Royal Society of Chemistry 2023-01-03 /pmc/articles/PMC9890556/ /pubmed/36755706 http://dx.doi.org/10.1039/d2sc05918e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Majhi, Jadab
Granados, Albert
Matsuo, Bianca
Ciccone, Vittorio
Dhungana, Roshan K.
Sharique, Mohammed
Molander, Gary A.
Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
title Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
title_full Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
title_fullStr Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
title_full_unstemmed Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
title_short Practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
title_sort practical, scalable, and transition metal-free visible light-induced heteroarylation route to substituted oxindoles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890556/
https://www.ncbi.nlm.nih.gov/pubmed/36755706
http://dx.doi.org/10.1039/d2sc05918e
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