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Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect
This review aims at providing an overview of the most significant applications of fluorine-containing ligands reported in the literature starting from 2001 until mid-2021. The ligands are classified according to the nature of the donor atoms involved. This review highlights both metal–ligand interac...
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/PMC9516955/ https://www.ncbi.nlm.nih.gov/pubmed/36320478 http://dx.doi.org/10.1039/d2sc01096h |
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author | Lauzon, Samuel Ollevier, Thierry |
author_facet | Lauzon, Samuel Ollevier, Thierry |
author_sort | Lauzon, Samuel |
collection | PubMed |
description | This review aims at providing an overview of the most significant applications of fluorine-containing ligands reported in the literature starting from 2001 until mid-2021. The ligands are classified according to the nature of the donor atoms involved. This review highlights both metal–ligand interactions and the structure–reactivity relationships resulting from the presence of the fluorine atom or fluorine-containing substituents on chiral catalysts. |
format | Online Article Text |
id | pubmed-9516955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-95169552022-10-31 Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect Lauzon, Samuel Ollevier, Thierry Chem Sci Chemistry This review aims at providing an overview of the most significant applications of fluorine-containing ligands reported in the literature starting from 2001 until mid-2021. The ligands are classified according to the nature of the donor atoms involved. This review highlights both metal–ligand interactions and the structure–reactivity relationships resulting from the presence of the fluorine atom or fluorine-containing substituents on chiral catalysts. The Royal Society of Chemistry 2022-08-08 /pmc/articles/PMC9516955/ /pubmed/36320478 http://dx.doi.org/10.1039/d2sc01096h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Lauzon, Samuel Ollevier, Thierry Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
title | Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
title_full | Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
title_fullStr | Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
title_full_unstemmed | Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
title_short | Fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
title_sort | fluorine in metal-catalyzed asymmetric transformations: the lightest halogen causing a massive effect |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516955/ https://www.ncbi.nlm.nih.gov/pubmed/36320478 http://dx.doi.org/10.1039/d2sc01096h |
work_keys_str_mv | AT lauzonsamuel fluorineinmetalcatalyzedasymmetrictransformationsthelightesthalogencausingamassiveeffect AT ollevierthierry fluorineinmetalcatalyzedasymmetrictransformationsthelightesthalogencausingamassiveeffect |