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Enantioselective Aromatic Amination?

The atroposelective formation of C−N bonds has recently emerged within the field of amination reactions. On first sight, it may seem quite surprising that such an ancient class of organic coupling reactions (Gabriel, Ullmann, Goldberg, Buchwald, Hartwig and many others) has so few enantioselective s...

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Detalles Bibliográficos
Autores principales: Thönnißen, Vinzenz, Patureau, Frederic W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252738/
https://www.ncbi.nlm.nih.gov/pubmed/33073420
http://dx.doi.org/10.1002/chem.202004151
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author Thönnißen, Vinzenz
Patureau, Frederic W.
author_facet Thönnißen, Vinzenz
Patureau, Frederic W.
author_sort Thönnißen, Vinzenz
collection PubMed
description The atroposelective formation of C−N bonds has recently emerged within the field of amination reactions. On first sight, it may seem quite surprising that such an ancient class of organic coupling reactions (Gabriel, Ullmann, Goldberg, Buchwald, Hartwig and many others) has so few enantioselective solutions, and this in spite of asymmetric synthesis being now a mature concept and field. Why should enantioselective C−N bond formation be so difficult? This question and some of the first examples that promise an imminent change of paradigm are herein discussed.
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spelling pubmed-82527382021-07-12 Enantioselective Aromatic Amination? Thönnißen, Vinzenz Patureau, Frederic W. Chemistry Concepts The atroposelective formation of C−N bonds has recently emerged within the field of amination reactions. On first sight, it may seem quite surprising that such an ancient class of organic coupling reactions (Gabriel, Ullmann, Goldberg, Buchwald, Hartwig and many others) has so few enantioselective solutions, and this in spite of asymmetric synthesis being now a mature concept and field. Why should enantioselective C−N bond formation be so difficult? This question and some of the first examples that promise an imminent change of paradigm are herein discussed. John Wiley and Sons Inc. 2021-03-11 2021-05-03 /pmc/articles/PMC8252738/ /pubmed/33073420 http://dx.doi.org/10.1002/chem.202004151 Text en © 2020 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Concepts
Thönnißen, Vinzenz
Patureau, Frederic W.
Enantioselective Aromatic Amination?
title Enantioselective Aromatic Amination?
title_full Enantioselective Aromatic Amination?
title_fullStr Enantioselective Aromatic Amination?
title_full_unstemmed Enantioselective Aromatic Amination?
title_short Enantioselective Aromatic Amination?
title_sort enantioselective aromatic amination?
topic Concepts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252738/
https://www.ncbi.nlm.nih.gov/pubmed/33073420
http://dx.doi.org/10.1002/chem.202004151
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