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Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade
Saturated N‐heterocycles are prominent motifs found in various natural products and pharmaceuticals. Despite the increasing interest in this class of compounds, the synthesis of saturated bicyclic azacycles requires tedious multi‐step syntheses. Herein, we present a one‐pot protocol for the synthesi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796080/ https://www.ncbi.nlm.nih.gov/pubmed/36589139 http://dx.doi.org/10.1002/adsc.202200601 |
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author | Wagener, Tobias Pierau, Marco Heusler, Arne Glorius, Frank |
author_facet | Wagener, Tobias Pierau, Marco Heusler, Arne Glorius, Frank |
author_sort | Wagener, Tobias |
collection | PubMed |
description | Saturated N‐heterocycles are prominent motifs found in various natural products and pharmaceuticals. Despite the increasing interest in this class of compounds, the synthesis of saturated bicyclic azacycles requires tedious multi‐step syntheses. Herein, we present a one‐pot protocol for the synthesis of octahydroindoles, decahydroquinolines, and octahydroindolizines through a cascade reaction. [Image: see text] |
format | Online Article Text |
id | pubmed-9796080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97960802022-12-28 Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade Wagener, Tobias Pierau, Marco Heusler, Arne Glorius, Frank Adv Synth Catal Communications Saturated N‐heterocycles are prominent motifs found in various natural products and pharmaceuticals. Despite the increasing interest in this class of compounds, the synthesis of saturated bicyclic azacycles requires tedious multi‐step syntheses. Herein, we present a one‐pot protocol for the synthesis of octahydroindoles, decahydroquinolines, and octahydroindolizines through a cascade reaction. [Image: see text] John Wiley and Sons Inc. 2022-06-23 2022-10-04 /pmc/articles/PMC9796080/ /pubmed/36589139 http://dx.doi.org/10.1002/adsc.202200601 Text en © 2022 The Authors. Advanced Synthesis & Catalysis 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 | Communications Wagener, Tobias Pierau, Marco Heusler, Arne Glorius, Frank Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade |
title | Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade |
title_full | Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade |
title_fullStr | Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade |
title_full_unstemmed | Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade |
title_short | Synthesis of Saturated N‐Heterocycles via a Catalytic Hydrogenation Cascade |
title_sort | synthesis of saturated n‐heterocycles via a catalytic hydrogenation cascade |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796080/ https://www.ncbi.nlm.nih.gov/pubmed/36589139 http://dx.doi.org/10.1002/adsc.202200601 |
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