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Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review

In this review, recent advances over the past decade in the preparation of fluorinated stereogenic quaternary centers on β-keto esters compounds are analyzed. Since the incorporation of fluorine and fluorinated groups is of special interest in pharmaceutical chemistry, a range of metal-catalyzed and...

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Autores principales: Granados, Albert, Vallribera, Adelina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397287/
https://www.ncbi.nlm.nih.gov/pubmed/32708946
http://dx.doi.org/10.3390/molecules25143264
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author Granados, Albert
Vallribera, Adelina
author_facet Granados, Albert
Vallribera, Adelina
author_sort Granados, Albert
collection PubMed
description In this review, recent advances over the past decade in the preparation of fluorinated stereogenic quaternary centers on β-keto esters compounds are analyzed. Since the incorporation of fluorine and fluorinated groups is of special interest in pharmaceutical chemistry, a range of metal-catalyzed and organocatalyzed methods have been developed. Herein, we review the enantioselective fluorination, trifluoromethylation and trifluoromethylthiolation of 3-oxo esters. The scope, the induction of enantioselectivity and mechanistic investigations are presented.
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spelling pubmed-73972872020-08-16 Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review Granados, Albert Vallribera, Adelina Molecules Review In this review, recent advances over the past decade in the preparation of fluorinated stereogenic quaternary centers on β-keto esters compounds are analyzed. Since the incorporation of fluorine and fluorinated groups is of special interest in pharmaceutical chemistry, a range of metal-catalyzed and organocatalyzed methods have been developed. Herein, we review the enantioselective fluorination, trifluoromethylation and trifluoromethylthiolation of 3-oxo esters. The scope, the induction of enantioselectivity and mechanistic investigations are presented. MDPI 2020-07-17 /pmc/articles/PMC7397287/ /pubmed/32708946 http://dx.doi.org/10.3390/molecules25143264 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Granados, Albert
Vallribera, Adelina
Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review
title Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review
title_full Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review
title_fullStr Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review
title_full_unstemmed Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review
title_short Asymmetric Preparation of α-Quaternary Fluorinated β-keto Esters. Review
title_sort asymmetric preparation of α-quaternary fluorinated β-keto esters. review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397287/
https://www.ncbi.nlm.nih.gov/pubmed/32708946
http://dx.doi.org/10.3390/molecules25143264
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