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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...

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Detalles Bibliográficos
Autores principales: Deolka, Shubham, Govindarajan, Ramadoss, Vasylevskyi, Serhii, Roy, Michael C., Khusnutdinova, Julia R., Khaskin, Eugene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
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.
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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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