Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts
文献类型：期刊论文
| 作者 | Han FS |
| 刊名 | chemical society reviews
 |
| 出版日期 | 2013 |
| 卷号 | 42期号:12页码:5270-5298 |
| 关键词 | SECONDARY ALKYL CHLORIDES ARYL BORONIC ACIDS C-O ACTIVATION HETEROCYCLIC CARBENE LIGAND DIRECTED ORTHO-METALATION AXIALLY CHIRAL BIARYLS CARBON BOND FORMATION ARYLBORONIC ACIDS ROOM-TEMPERATURE GRIGNARD-REAGENTS |
| ISSN号 | 0306-0012 |
| 通讯作者 | han fs |
| 中文摘要 | in the transition-metal-catalyzed cross-coupling reactions, the use of the first row transition metals as catalysts is much more appealing than the precious metals owing to the apparent advantages such as cheapness and earth abundance. within the last two decades, particularly the last five years, explosive interests have been focused on the nickel-catalyzed suzuki-miyaura reactions. this has greatly advanced the chemistry of transition-metal-catalyzed cross-coupling reactions. most notably, a broad range of aryl electrophiles such as phenols, aryl ethers, esters, carbonates, carbamates, sulfamates, phosphates, phosphoramides, phosphonium salts, and fluorides, as well as various alkyl electrophiles, which are conventionally challenging, by applying palladium catalysts can now be coupled efficiently with boron reagents in the presence of nickel catalysts. in this review, we would like to summarize the progress in this reaction. |
| 收录类别 | SCI收录期刊论文 |
| 语种 | 英语 |
| WOS记录号 | WOS:000319527400028 |
| 公开日期 | 2014-04-18 |
| 源URL | [http://ir.ciac.jl.cn/handle/322003/50273]  |
| 专题 | 长春应用化学研究所_长春应用化学研究所知识产出_期刊论文 |
| 推荐引用方式 GB/T 7714 | Han FS. Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts[J]. chemical society reviews,2013,42(12):5270-5298. |
| APA | Han FS.(2013).Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts.chemical society reviews,42(12),5270-5298. |
| MLA | Han FS."Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts".chemical society reviews 42.12(2013):5270-5298. |
入库方式： OAI收割
来源：长春应用化学研究所
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