Readily available phosphine-phosphoramidite ligands for highly efficient Rh-catalyzed enantioselective hydrogenations
文献类型:期刊论文
作者 | Huang, Jia-Di; Hu, Xiang-Ping; Duan, Zheng-Chao; Zeng, Qing-Hen; Yu, Sai-Bo; Deng, Jun; Wang, Dao-Yong; Zheng, Zhuo |
刊名 | organic letters
![]() |
出版日期 | 2006-09-14 |
卷号 | 8期号:19页码:4367-4370 |
产权排序 | 1;1 |
通讯作者 | 郑卓 |
英文摘要 | a new family of air- and moisture-stable phosphine-phosphoramidite ligands (peaphos) has been prepared from commercially available and inexpensive ( s)-alpha-phenylethylamine through a two- or three-step transformation and successfully applied in the rhodium-catalyzed enantioselective hydrogenations of a variety of substrates, in which up to 99.9% ee was obtained for all of these kinds of substrates. |
WOS标题词 | science & technology ; physical sciences |
类目[WOS] | chemistry, organic |
研究领域[WOS] | chemistry |
关键词[WOS] | phenylethylamine alpha-pea ; asymmetric hydrogenation ; enantiopure compounds ; ferrocenyl ligands ; phosphorus ligands ; acid-derivatives ; complexes ; quinaphos |
收录类别 | SCI ; IC ; CCR |
原文出处 | true |
语种 | 英语 |
WOS记录号 | WOS:000240339700049 |
公开日期 | 2010-11-30 |
源URL | [http://159.226.238.44/handle/321008/98095] ![]() |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
作者单位 | 1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China 2.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China |
推荐引用方式 GB/T 7714 | Huang, Jia-Di,Hu, Xiang-Ping,Duan, Zheng-Chao,et al. Readily available phosphine-phosphoramidite ligands for highly efficient Rh-catalyzed enantioselective hydrogenations[J]. organic letters,2006,8(19):4367-4370. |
APA | Huang, Jia-Di.,Hu, Xiang-Ping.,Duan, Zheng-Chao.,Zeng, Qing-Hen.,Yu, Sai-Bo.,...&Zheng, Zhuo.(2006).Readily available phosphine-phosphoramidite ligands for highly efficient Rh-catalyzed enantioselective hydrogenations.organic letters,8(19),4367-4370. |
MLA | Huang, Jia-Di,et al."Readily available phosphine-phosphoramidite ligands for highly efficient Rh-catalyzed enantioselective hydrogenations".organic letters 8.19(2006):4367-4370. |
入库方式: OAI收割
来源:大连化学物理研究所
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。