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Asymmetric synthesis of highly sterically congested α-tertiary amines via organocatalyzed kinetic resolution | |
2023 | |
发表期刊 | CHEMICAL COMMUNICATIONS (IF:4.3[JCR-2023],4.4[5-Year]) |
ISSN | 1359-7345 |
EISSN | 1364-548X |
卷号 | 59期号:32页码:4762-4765 |
发表状态 | 已发表 |
DOI | 10.1039/d3cc00653k |
摘要 | The asymmetric synthesis of highly sterically congested α-tertiary amines was achieved by an organocatalyzed kinetic resolution (KR) protocol, which were otherwise difficult to access. A variety of substituted N-aryl α-tertiary amines bearing 2-substitued phenyl groups were kinetically resolved through the asymmetric C-H amination reaction, affording good to high KR performances. © 2023 The Royal Society of Chemistry. |
关键词 | Amines Amination reaction Asymmetric synthesis C-H amination Kinetic resolution Performance Phenyl group Sterically congested Tertiary amine |
URL | 查看原文 |
收录类别 | SCI ; EI |
语种 | 英语 |
资助项目 | NSFC[ |
WOS研究方向 | Chemistry |
WOS类目 | Chemistry, Multidisciplinary |
WOS记录号 | WOS:000968496000001 |
出版者 | Royal Society of Chemistry |
EI入藏号 | 20231513872436 |
EI主题词 | Kinetics |
EI分类号 | 631.1 Fluid Flow, General ; 804.1 Organic Compounds ; 931 Classical Physics ; Quantum Theory ; Relativity |
原始文献类型 | Article in Press |
引用统计 | 正在获取...
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文献类型 | 期刊论文 |
条目标识符 | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/297908 |
专题 | 物质科学与技术学院 物质科学与技术学院_PI研究组_杨晓瑜组 物质科学与技术学院_硕士生 物质科学与技术学院_博士生 |
通讯作者 | Yang, Xiaoyu |
作者单位 | ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China |
第一作者单位 | 物质科学与技术学院 |
通讯作者单位 | 物质科学与技术学院 |
第一作者的第一单位 | 物质科学与技术学院 |
推荐引用方式 GB/T 7714 | Jiang, Qianwen,Xie, Wansen,Yang, Xiaoyu. Asymmetric synthesis of highly sterically congested α-tertiary amines via organocatalyzed kinetic resolution[J]. CHEMICAL COMMUNICATIONS,2023,59(32):4762-4765. |
APA | Jiang, Qianwen,Xie, Wansen,&Yang, Xiaoyu.(2023).Asymmetric synthesis of highly sterically congested α-tertiary amines via organocatalyzed kinetic resolution.CHEMICAL COMMUNICATIONS,59(32),4762-4765. |
MLA | Jiang, Qianwen,et al."Asymmetric synthesis of highly sterically congested α-tertiary amines via organocatalyzed kinetic resolution".CHEMICAL COMMUNICATIONS 59.32(2023):4762-4765. |
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