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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8252738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT thonnißenvinzenz enantioselectivearomaticamination AT patureaufredericw enantioselectivearomaticamination |