Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides
文献类型:期刊论文
作者 | Lai, Yi1; Zong, Zhijian1; Tang, Yujie1; Mo, Weimin1; Sun, Nan1; Hu, Baoxiang1; Shen, Zhenlu1; Jin, Liqun1,2; Sun, Wen-hua3,4![]() |
刊名 | BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
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出版日期 | 2017-02-03 |
卷号 | 13页码:213-221 |
关键词 | Aryl Chloride Geometry-constrained Iminopyridyl Palladium Suzuki |
英文摘要 | A series of bulky geometry-constrained iminopyridylpalladium chlorides were developed. The steric environment adjacent to the nitrogen atom in the pyridine rings and diimine parts enhanced the thermal stability of the palladium species. Bulkier groups at the imino group stabilized the palladium species and the corresponding palladium chlorides showed high activities in the coupling reaction of aryl chlorides. |
语种 | 英语 |
源URL | [http://ir.iccas.ac.cn/handle/121111/38203] ![]() |
专题 | 化学研究所_工程塑料实验室 |
作者单位 | 1.Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310032, Zhejiang, Peoples R China 2.Chinese Acad Sci, State Key Lab Oxo Synth & Select Oxidat, Lanzhou Inst Chem Phys, Lanzhou 730000, Peoples R China 3.Chinese Acad Sci, Key Lab Engn Plast, Inst Chem, Beijing 100190, Peoples R China 4.Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100190, Peoples R China |
推荐引用方式 GB/T 7714 | Lai, Yi,Zong, Zhijian,Tang, Yujie,et al. Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides[J]. BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY,2017,13:213-221. |
APA | Lai, Yi.,Zong, Zhijian.,Tang, Yujie.,Mo, Weimin.,Sun, Nan.,...&Hu, Xinquan.(2017).Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides.BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY,13,213-221. |
MLA | Lai, Yi,et al."Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides".BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY 13(2017):213-221. |
入库方式: OAI收割
来源:化学研究所
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