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Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds

In recent years, the synthesis of axially chiral compounds has received considerable attention due to their extensive application as biologically active compounds in medicinal chemistry and as chiral ligands in asymmetric catalysis. Chiral phosphoric acids are recognized as efficient organocatalysts...

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Detalles Bibliográficos
Autores principales: Woldegiorgis, Alemayehu Gashaw, Lin, Xufeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609246/
https://www.ncbi.nlm.nih.gov/pubmed/34876929
http://dx.doi.org/10.3762/bjoc.17.185
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author Woldegiorgis, Alemayehu Gashaw
Lin, Xufeng
author_facet Woldegiorgis, Alemayehu Gashaw
Lin, Xufeng
author_sort Woldegiorgis, Alemayehu Gashaw
collection PubMed
description In recent years, the synthesis of axially chiral compounds has received considerable attention due to their extensive application as biologically active compounds in medicinal chemistry and as chiral ligands in asymmetric catalysis. Chiral phosphoric acids are recognized as efficient organocatalysts for a variety of enantioselective transformations. In this review, we summarize the recent development of chiral phosphoric acid-catalyzed synthesis of a wide range of axially chiral biaryls, heterobiaryls, vinylarenes, N-arylamines, spiranes, and allenes with high efficiency and excellent stereoselectivity.
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spelling pubmed-86092462021-12-06 Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds Woldegiorgis, Alemayehu Gashaw Lin, Xufeng Beilstein J Org Chem Review In recent years, the synthesis of axially chiral compounds has received considerable attention due to their extensive application as biologically active compounds in medicinal chemistry and as chiral ligands in asymmetric catalysis. Chiral phosphoric acids are recognized as efficient organocatalysts for a variety of enantioselective transformations. In this review, we summarize the recent development of chiral phosphoric acid-catalyzed synthesis of a wide range of axially chiral biaryls, heterobiaryls, vinylarenes, N-arylamines, spiranes, and allenes with high efficiency and excellent stereoselectivity. Beilstein-Institut 2021-11-15 /pmc/articles/PMC8609246/ /pubmed/34876929 http://dx.doi.org/10.3762/bjoc.17.185 Text en Copyright © 2021, Woldegiorgis and Lin https://creativecommons.org/licenses/by/4.0/https://www.beilstein-journals.org/bjoc/terms/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms/terms)
spellingShingle Review
Woldegiorgis, Alemayehu Gashaw
Lin, Xufeng
Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
title Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
title_full Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
title_fullStr Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
title_full_unstemmed Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
title_short Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
title_sort recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8609246/
https://www.ncbi.nlm.nih.gov/pubmed/34876929
http://dx.doi.org/10.3762/bjoc.17.185
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