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Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)

Over the years, the development of new methodologies for the introduction of various fluorinated motifs has gained a significant interest due to the importance of fluorine-containing molecules in the pharmaceutical and agrochemical industries. In a world eager to eco-friendlier tools, the need for i...

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Autores principales: Ruyet, Louise, Besset, Tatiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277540/
https://www.ncbi.nlm.nih.gov/pubmed/32550920
http://dx.doi.org/10.3762/bjoc.16.92
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author Ruyet, Louise
Besset, Tatiana
author_facet Ruyet, Louise
Besset, Tatiana
author_sort Ruyet, Louise
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description Over the years, the development of new methodologies for the introduction of various fluorinated motifs has gained a significant interest due to the importance of fluorine-containing molecules in the pharmaceutical and agrochemical industries. In a world eager to eco-friendlier tools, the need for innovative methods has been growing. To address these two challenges, copper-based reagents were developed to introduce CF(2)H, CF(2)R(F), CF(2)CH(3), CF(2)PO(OEt)(2) and CF(2)SO(2)Ph motifs on a broad range of substrates. Copper-based fluorinated reagents have the advantage of being inexpensive and generally in situ generated or prepared in a few steps, which make them convenient to use. In this review, an overview of the recent advances made for the synthesis of fluorinated molecules using copper-based fluorinated reagents will be given.
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spelling pubmed-72775402020-06-17 Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F) Ruyet, Louise Besset, Tatiana Beilstein J Org Chem Review Over the years, the development of new methodologies for the introduction of various fluorinated motifs has gained a significant interest due to the importance of fluorine-containing molecules in the pharmaceutical and agrochemical industries. In a world eager to eco-friendlier tools, the need for innovative methods has been growing. To address these two challenges, copper-based reagents were developed to introduce CF(2)H, CF(2)R(F), CF(2)CH(3), CF(2)PO(OEt)(2) and CF(2)SO(2)Ph motifs on a broad range of substrates. Copper-based fluorinated reagents have the advantage of being inexpensive and generally in situ generated or prepared in a few steps, which make them convenient to use. In this review, an overview of the recent advances made for the synthesis of fluorinated molecules using copper-based fluorinated reagents will be given. Beilstein-Institut 2020-05-18 /pmc/articles/PMC7277540/ /pubmed/32550920 http://dx.doi.org/10.3762/bjoc.16.92 Text en Copyright © 2020, Ruyet and Besset 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). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Ruyet, Louise
Besset, Tatiana
Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)
title Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)
title_full Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)
title_fullStr Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)
title_full_unstemmed Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)
title_short Copper-based fluorinated reagents for the synthesis of CF(2)R-containing molecules (R ≠ F)
title_sort copper-based fluorinated reagents for the synthesis of cf(2)r-containing molecules (r ≠ f)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277540/
https://www.ncbi.nlm.nih.gov/pubmed/32550920
http://dx.doi.org/10.3762/bjoc.16.92
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