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Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes
We describe a “ligand-free” Ni-catalyzed perfluoroalkylation of heteroarenes to produce a diverse array of trfiluoromethyl, pentafluoroethyl and heptafluoropropyl adducts. Catalysis proceeds at room temperature via a radical pathway. The catalytic protocol is distinguished by its simplicity, and its...
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/PMC9667918/ https://www.ncbi.nlm.nih.gov/pubmed/36425484 http://dx.doi.org/10.1039/d2sc03879j |
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author | Deolka, Shubham Govindarajan, Ramadoss Vasylevskyi, Serhii Roy, Michael C. Khusnutdinova, Julia R. Khaskin, Eugene |
author_facet | Deolka, Shubham Govindarajan, Ramadoss Vasylevskyi, Serhii Roy, Michael C. Khusnutdinova, Julia R. Khaskin, Eugene |
author_sort | Deolka, Shubham |
collection | PubMed |
description | We describe a “ligand-free” Ni-catalyzed perfluoroalkylation of heteroarenes to produce a diverse array of trfiluoromethyl, pentafluoroethyl and heptafluoropropyl adducts. Catalysis proceeds at room temperature via a radical pathway. The catalytic protocol is distinguished by its simplicity, and its wide scope demonstrates the potential in the late-stage functionalization of drug analogues and peptides. |
format | Online Article Text |
id | pubmed-9667918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-96679182022-11-23 Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes Deolka, Shubham Govindarajan, Ramadoss Vasylevskyi, Serhii Roy, Michael C. Khusnutdinova, Julia R. Khaskin, Eugene Chem Sci Chemistry We describe a “ligand-free” Ni-catalyzed perfluoroalkylation of heteroarenes to produce a diverse array of trfiluoromethyl, pentafluoroethyl and heptafluoropropyl adducts. Catalysis proceeds at room temperature via a radical pathway. The catalytic protocol is distinguished by its simplicity, and its wide scope demonstrates the potential in the late-stage functionalization of drug analogues and peptides. The Royal Society of Chemistry 2022-10-17 /pmc/articles/PMC9667918/ /pubmed/36425484 http://dx.doi.org/10.1039/d2sc03879j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Deolka, Shubham Govindarajan, Ramadoss Vasylevskyi, Serhii Roy, Michael C. Khusnutdinova, Julia R. Khaskin, Eugene Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
title | Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
title_full | Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
title_fullStr | Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
title_full_unstemmed | Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
title_short | Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
title_sort | ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667918/ https://www.ncbi.nlm.nih.gov/pubmed/36425484 http://dx.doi.org/10.1039/d2sc03879j |
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