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NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles
A practical NaI/PPh(3)-catalyzed decarboxylative radical cascade cyclization of N-arylacrylamides with redox-active esters is described, which is mediated by visible light irradiation. A wide range of substrates bearing different substituents and derived from ubiquitous carboxylic acids, including α...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874234/ https://www.ncbi.nlm.nih.gov/pubmed/36741816 http://dx.doi.org/10.3762/bjoc.19.5 |
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author | Liu, Dan Zhao, Yue Patureau, Frederic W |
author_facet | Liu, Dan Zhao, Yue Patureau, Frederic W |
author_sort | Liu, Dan |
collection | PubMed |
description | A practical NaI/PPh(3)-catalyzed decarboxylative radical cascade cyclization of N-arylacrylamides with redox-active esters is described, which is mediated by visible light irradiation. A wide range of substrates bearing different substituents and derived from ubiquitous carboxylic acids, including α-amino acids, were synthesized and examined under this very mild, efficient, and cost effective transition-metal-free synthetic method. These afforded various functionalized oxindoles featuring a C3 quaternary stereogenic center. Mechanistic experiments suggest a radical mechanism. |
format | Online Article Text |
id | pubmed-9874234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-98742342023-02-02 NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles Liu, Dan Zhao, Yue Patureau, Frederic W Beilstein J Org Chem Letter A practical NaI/PPh(3)-catalyzed decarboxylative radical cascade cyclization of N-arylacrylamides with redox-active esters is described, which is mediated by visible light irradiation. A wide range of substrates bearing different substituents and derived from ubiquitous carboxylic acids, including α-amino acids, were synthesized and examined under this very mild, efficient, and cost effective transition-metal-free synthetic method. These afforded various functionalized oxindoles featuring a C3 quaternary stereogenic center. Mechanistic experiments suggest a radical mechanism. Beilstein-Institut 2023-01-16 /pmc/articles/PMC9874234/ /pubmed/36741816 http://dx.doi.org/10.3762/bjoc.19.5 Text en Copyright © 2023, Liu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Letter Liu, Dan Zhao, Yue Patureau, Frederic W NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles |
title | NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles |
title_full | NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles |
title_fullStr | NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles |
title_full_unstemmed | NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles |
title_short | NaI/PPh(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of N-arylacrylamides for the efficient synthesis of quaternary oxindoles |
title_sort | nai/pph(3)-catalyzed visible-light-mediated decarboxylative radical cascade cyclization of n-arylacrylamides for the efficient synthesis of quaternary oxindoles |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874234/ https://www.ncbi.nlm.nih.gov/pubmed/36741816 http://dx.doi.org/10.3762/bjoc.19.5 |
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