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Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer
Sulfoximines are synthetically important scaffolds and serve important roles in drug discovery. Currently, there is no solution to decarboxylative sulfoximination of benzoic acids; although thoroughly investigated, limited substrate scope and harsh reaction conditions still hold back traditional the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682917/ https://www.ncbi.nlm.nih.gov/pubmed/36507153 http://dx.doi.org/10.1039/d2sc05442f |
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author | Xu, Peng Su, Wanqi Ritter, Tobias |
author_facet | Xu, Peng Su, Wanqi Ritter, Tobias |
author_sort | Xu, Peng |
collection | PubMed |
description | Sulfoximines are synthetically important scaffolds and serve important roles in drug discovery. Currently, there is no solution to decarboxylative sulfoximination of benzoic acids; although thoroughly investigated, limited substrate scope and harsh reaction conditions still hold back traditional thermal aromatic decarboxylative functionalization. Herein, we realize the first decarboxylative sulfoximination of benzoic acids via photo-induced ligand to copper charge transfer (copper-LMCT)-enabled decarboxylative carbometalation. The transformation proceeds under mild reaction conditions, has a broad substrate scope, and can be applied to late-stage functionalization of complex small molecules. |
format | Online Article Text |
id | pubmed-9682917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-96829172022-12-08 Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer Xu, Peng Su, Wanqi Ritter, Tobias Chem Sci Chemistry Sulfoximines are synthetically important scaffolds and serve important roles in drug discovery. Currently, there is no solution to decarboxylative sulfoximination of benzoic acids; although thoroughly investigated, limited substrate scope and harsh reaction conditions still hold back traditional thermal aromatic decarboxylative functionalization. Herein, we realize the first decarboxylative sulfoximination of benzoic acids via photo-induced ligand to copper charge transfer (copper-LMCT)-enabled decarboxylative carbometalation. The transformation proceeds under mild reaction conditions, has a broad substrate scope, and can be applied to late-stage functionalization of complex small molecules. The Royal Society of Chemistry 2022-11-14 /pmc/articles/PMC9682917/ /pubmed/36507153 http://dx.doi.org/10.1039/d2sc05442f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Xu, Peng Su, Wanqi Ritter, Tobias Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
title | Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
title_full | Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
title_fullStr | Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
title_full_unstemmed | Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
title_short | Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
title_sort | decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682917/ https://www.ncbi.nlm.nih.gov/pubmed/36507153 http://dx.doi.org/10.1039/d2sc05442f |
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