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Imide arylation with aryl(TMP)iodonium tosylates

Herein, we describe the synthesis of N-aryl phthalimides by metal-free coupling of potassium phthalimide with unsymmetrical aryl(TMP)iodonium tosylate salts. The aryl transfer from the iodonium moiety occurs under electronic control with the electron-rich trimethoxyphenyl group acting as a competent...

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Detalles Bibliográficos
Autores principales: Basu, Souradeep, Sandtorv, Alexander H, Stuart, David R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009222/
https://www.ncbi.nlm.nih.gov/pubmed/29977376
http://dx.doi.org/10.3762/bjoc.14.90
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author Basu, Souradeep
Sandtorv, Alexander H
Stuart, David R
author_facet Basu, Souradeep
Sandtorv, Alexander H
Stuart, David R
author_sort Basu, Souradeep
collection PubMed
description Herein, we describe the synthesis of N-aryl phthalimides by metal-free coupling of potassium phthalimide with unsymmetrical aryl(TMP)iodonium tosylate salts. The aryl transfer from the iodonium moiety occurs under electronic control with the electron-rich trimethoxyphenyl group acting as a competent dummy ligand. The yields of N-aryl phthalimides are moderate to high and the coupling reaction is compatible with electron-deficient and sterically encumbered aryl groups.
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spelling pubmed-60092222018-07-05 Imide arylation with aryl(TMP)iodonium tosylates Basu, Souradeep Sandtorv, Alexander H Stuart, David R Beilstein J Org Chem Letter Herein, we describe the synthesis of N-aryl phthalimides by metal-free coupling of potassium phthalimide with unsymmetrical aryl(TMP)iodonium tosylate salts. The aryl transfer from the iodonium moiety occurs under electronic control with the electron-rich trimethoxyphenyl group acting as a competent dummy ligand. The yields of N-aryl phthalimides are moderate to high and the coupling reaction is compatible with electron-deficient and sterically encumbered aryl groups. Beilstein-Institut 2018-05-11 /pmc/articles/PMC6009222/ /pubmed/29977376 http://dx.doi.org/10.3762/bjoc.14.90 Text en Copyright © 2018, Basu et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Basu, Souradeep
Sandtorv, Alexander H
Stuart, David R
Imide arylation with aryl(TMP)iodonium tosylates
title Imide arylation with aryl(TMP)iodonium tosylates
title_full Imide arylation with aryl(TMP)iodonium tosylates
title_fullStr Imide arylation with aryl(TMP)iodonium tosylates
title_full_unstemmed Imide arylation with aryl(TMP)iodonium tosylates
title_short Imide arylation with aryl(TMP)iodonium tosylates
title_sort imide arylation with aryl(tmp)iodonium tosylates
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009222/
https://www.ncbi.nlm.nih.gov/pubmed/29977376
http://dx.doi.org/10.3762/bjoc.14.90
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