Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783333333000781824 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6009222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT basusouradeep imidearylationwitharyltmpiodoniumtosylates AT sandtorvalexanderh imidearylationwitharyltmpiodoniumtosylates AT stuartdavidr imidearylationwitharyltmpiodoniumtosylates |