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Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage
A one-pot synthesis, initiated by a copper salt with inorganic (NH(4))(2)CO(3) as the nitrogen source, forms divergent aryl imidazole derivatives from ketones via α-amination and oxidative C–C bond cleavage reactions. The approach provides a simple and rapid synthesis of imidazole derivatives and ha...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051655/ https://www.ncbi.nlm.nih.gov/pubmed/35492973 http://dx.doi.org/10.1039/d0ra01408g |
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author | Huang, Jiangkun Luo, Lan Xing, Naiguo Gu, Linghui Li, Chen Han, Qiao Zheng, Shilong He, Ling |
author_facet | Huang, Jiangkun Luo, Lan Xing, Naiguo Gu, Linghui Li, Chen Han, Qiao Zheng, Shilong He, Ling |
author_sort | Huang, Jiangkun |
collection | PubMed |
description | A one-pot synthesis, initiated by a copper salt with inorganic (NH(4))(2)CO(3) as the nitrogen source, forms divergent aryl imidazole derivatives from ketones via α-amination and oxidative C–C bond cleavage reactions. The approach provides a simple and rapid synthesis of imidazole derivatives and has certain versatility. |
format | Online Article Text |
id | pubmed-9051655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90516552022-04-29 Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage Huang, Jiangkun Luo, Lan Xing, Naiguo Gu, Linghui Li, Chen Han, Qiao Zheng, Shilong He, Ling RSC Adv Chemistry A one-pot synthesis, initiated by a copper salt with inorganic (NH(4))(2)CO(3) as the nitrogen source, forms divergent aryl imidazole derivatives from ketones via α-amination and oxidative C–C bond cleavage reactions. The approach provides a simple and rapid synthesis of imidazole derivatives and has certain versatility. The Royal Society of Chemistry 2020-04-06 /pmc/articles/PMC9051655/ /pubmed/35492973 http://dx.doi.org/10.1039/d0ra01408g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Huang, Jiangkun Luo, Lan Xing, Naiguo Gu, Linghui Li, Chen Han, Qiao Zheng, Shilong He, Ling Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage |
title | Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage |
title_full | Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage |
title_fullStr | Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage |
title_full_unstemmed | Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage |
title_short | Novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative C–C bond cleavage |
title_sort | novel synthesis of divergent aryl imidazoles from ketones involving copper-catalyzed α-amination and oxidative c–c bond cleavage |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051655/ https://www.ncbi.nlm.nih.gov/pubmed/35492973 http://dx.doi.org/10.1039/d0ra01408g |
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