Journal article
Suzuki-Miyaura cross-coupling reaction of aryl chlorides with aryl boronic acids catalyzed by a palladium dichloride adduct of N-diphenylphosphanyl-2-aminopyridine
Tetrahedron, Vol.73(22), pp.3125-3132
2017
Abstract
One palladium dichloride adduct of a phosphine-pyridine ligand N-diphenylphosphanyl-2-aminopyridine (L1) [(L1)PdCl2] (1) has been prepared and structurally characterized. Compound 1 can be used as an effective catalyst for the Suzuki-Miyaura cross-coupling reactions of unreactive aryl chlorides with aryl boronic acids, and worked much better than its mono- or bidentate phosphine ligands. The reactions with a wide scope of substrates proceeded to give desired products in good to excellent yields.
Details
- Title
- Suzuki-Miyaura cross-coupling reaction of aryl chlorides with aryl boronic acids catalyzed by a palladium dichloride adduct of N-diphenylphosphanyl-2-aminopyridine
- Authors
- Lin-Yan Xu (Author) - Soochow University, ChinaChun-Yu Liu (Author) - Soochow University, ChinaShi-Yuan Liu (Author) - Soochow University, ChinaZhi-Gang Ren (Author) - Soochow University, ChinaDavid James Young (Author) - University of the Sunshine Coast - Faculty of Science, Health, Education and EngineeringJian-Ping Lang (Author) - Soochow University, China
- Publication details
- Tetrahedron, Vol.73(22), pp.3125-3132
- Publisher
- Pergamon
- Date published
- 2017
- DOI
- 10.1016/j.tet.2017.04.034
- ISSN
- 0040-4020; 0040-4020
- Copyright note
- Copyright © 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
- Organisation Unit
- University of the Sunshine Coast, Queensland
- Language
- English
- Record Identifier
- 99450443002621
- Output Type
- Journal article
- Research Statement
- false
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- Collaboration types
- Domestic collaboration
- International collaboration
- Web Of Science research areas
- Chemistry, Organic