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Construction of Phenanthridinone Skeletons through Palladium-Catalyzed Annulation
[Image: see text] Herein, a straightforward synthetic approach for the construction of phenanthridin-6(5H)-one skeletons is disclosed. The developed protocol relies on palladium catalysis, providing controlled access to a range of functionalized phenanthridin-6(5H)-ones in 59–88% yields. Furthermore...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476191/ https://www.ncbi.nlm.nih.gov/pubmed/37611263 http://dx.doi.org/10.1021/acs.joc.3c01429 |
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author | Geng, Xin He, Heng Shatskiy, Andrey Stepanova, Elena V. Alvey, Gregory R. Liu, Jian-Quan Kärkäs, Markus D. Wang, Xiang-Shan |
author_facet | Geng, Xin He, Heng Shatskiy, Andrey Stepanova, Elena V. Alvey, Gregory R. Liu, Jian-Quan Kärkäs, Markus D. Wang, Xiang-Shan |
author_sort | Geng, Xin |
collection | PubMed |
description | [Image: see text] Herein, a straightforward synthetic approach for the construction of phenanthridin-6(5H)-one skeletons is disclosed. The developed protocol relies on palladium catalysis, providing controlled access to a range of functionalized phenanthridin-6(5H)-ones in 59–88% yields. Furthermore, plausible reaction pathways are proposed based on mechanistic experiments. |
format | Online Article Text |
id | pubmed-10476191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104761912023-09-05 Construction of Phenanthridinone Skeletons through Palladium-Catalyzed Annulation Geng, Xin He, Heng Shatskiy, Andrey Stepanova, Elena V. Alvey, Gregory R. Liu, Jian-Quan Kärkäs, Markus D. Wang, Xiang-Shan J Org Chem [Image: see text] Herein, a straightforward synthetic approach for the construction of phenanthridin-6(5H)-one skeletons is disclosed. The developed protocol relies on palladium catalysis, providing controlled access to a range of functionalized phenanthridin-6(5H)-ones in 59–88% yields. Furthermore, plausible reaction pathways are proposed based on mechanistic experiments. American Chemical Society 2023-08-23 /pmc/articles/PMC10476191/ /pubmed/37611263 http://dx.doi.org/10.1021/acs.joc.3c01429 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Geng, Xin He, Heng Shatskiy, Andrey Stepanova, Elena V. Alvey, Gregory R. Liu, Jian-Quan Kärkäs, Markus D. Wang, Xiang-Shan Construction of Phenanthridinone Skeletons through Palladium-Catalyzed Annulation |
title | Construction of
Phenanthridinone Skeletons through
Palladium-Catalyzed Annulation |
title_full | Construction of
Phenanthridinone Skeletons through
Palladium-Catalyzed Annulation |
title_fullStr | Construction of
Phenanthridinone Skeletons through
Palladium-Catalyzed Annulation |
title_full_unstemmed | Construction of
Phenanthridinone Skeletons through
Palladium-Catalyzed Annulation |
title_short | Construction of
Phenanthridinone Skeletons through
Palladium-Catalyzed Annulation |
title_sort | construction of
phenanthridinone skeletons through
palladium-catalyzed annulation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476191/ https://www.ncbi.nlm.nih.gov/pubmed/37611263 http://dx.doi.org/10.1021/acs.joc.3c01429 |
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