中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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。