Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime
We first reported the new application of a translate metal chelating ligand α-benzoin oxime for improving Cu-catalyzed C-N coupling reactions. The system could catalyse coupling reactions of (hetero)aryl halides with a wide of nucleophiles (e.g., azoles, piperidine, pyrrolidine and amino ac...
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2019-11-01
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Online Access: | https://www.mdpi.com/1420-3049/24/22/4177 |
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doaj-716f0cb809264e2e9457bd53327adefb2020-11-25T02:21:51ZengMDPI AGMolecules1420-30492019-11-012422417710.3390/molecules24224177molecules24224177Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin OximeChunling Yuan0Lei Zhang1Yingdai Zhao2Department of Medicinal Chemistry, Pharmacy School, Jinzhou Medical University, Jinzhou 121001, ChinaDepartment of Medicinal Chemistry, Pharmacy School, Jinzhou Medical University, Jinzhou 121001, ChinaDepartment of Medicinal Chemistry, Pharmacy School, Jinzhou Medical University, Jinzhou 121001, ChinaWe first reported the new application of a translate metal chelating ligand α-benzoin oxime for improving Cu-catalyzed C-N coupling reactions. The system could catalyse coupling reactions of (hetero)aryl halides with a wide of nucleophiles (e.g., azoles, piperidine, pyrrolidine and amino acids) in moderate to excellent yields. The protocol allows rapid access to the most common scaffolds found in FDA-approved pharmaceuticals.https://www.mdpi.com/1420-3049/24/22/4177α-benzoin oximecopper catalyst(hetero)aryl halides<i>n</i>-nucleophilesc-n coupling |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chunling Yuan Lei Zhang Yingdai Zhao |
spellingShingle |
Chunling Yuan Lei Zhang Yingdai Zhao Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime Molecules α-benzoin oxime copper catalyst (hetero)aryl halides <i>n</i>-nucleophiles c-n coupling |
author_facet |
Chunling Yuan Lei Zhang Yingdai Zhao |
author_sort |
Chunling Yuan |
title |
Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime |
title_short |
Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime |
title_full |
Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime |
title_fullStr |
Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime |
title_full_unstemmed |
Cu(II)-Catalyzed C-N Coupling of (Hetero)aryl Halides and <i>N</i>-Nucleophiles Promoted by <i>α</i>-Benzoin Oxime |
title_sort |
cu(ii)-catalyzed c-n coupling of (hetero)aryl halides and <i>n</i>-nucleophiles promoted by <i>α</i>-benzoin oxime |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2019-11-01 |
description |
We first reported the new application of a translate metal chelating ligand α-benzoin oxime for improving Cu-catalyzed C-N coupling reactions. The system could catalyse coupling reactions of (hetero)aryl halides with a wide of nucleophiles (e.g., azoles, piperidine, pyrrolidine and amino acids) in moderate to excellent yields. The protocol allows rapid access to the most common scaffolds found in FDA-approved pharmaceuticals. |
topic |
α-benzoin oxime copper catalyst (hetero)aryl halides <i>n</i>-nucleophiles c-n coupling |
url |
https://www.mdpi.com/1420-3049/24/22/4177 |
work_keys_str_mv |
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_version_ |
1724865094698926080 |