中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
B(C6F5)(3)-catalyzed transfer hydrogenations of imines with Hantzsch esters

文献类型:期刊论文

作者Wang, Qiaotian1,2; Chen, Jingjing1,2; Feng, Xiangqing1,2; Du, Haifeng1,2
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
出版日期2018-03-07
卷号16期号:9页码:1448-1451
ISSN号1477-0520
DOI10.1039/c8ob00023a
英文摘要Highly efficient transfer hydrogenations of imines were realized with as low as 0.1 mol% of B(C6F5)(3) by using Hantzsch esters as a hydrogen source, furnishing a variety of amines in 80-99% yields. For the asymmetric transfer hydrogenations, up to 38% ee was obtained with chiral diene-derived boron Lewis acids.
语种英语
WOS记录号WOS:000429266600005
出版者ROYAL SOC CHEMISTRY
源URL[http://ir.iccas.ac.cn/handle/121111/46187]  
专题中国科学院化学研究所
通讯作者Feng, Xiangqing; Du, Haifeng
作者单位1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Wang, Qiaotian,Chen, Jingjing,Feng, Xiangqing,et al. B(C6F5)(3)-catalyzed transfer hydrogenations of imines with Hantzsch esters[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2018,16(9):1448-1451.
APA Wang, Qiaotian,Chen, Jingjing,Feng, Xiangqing,&Du, Haifeng.(2018).B(C6F5)(3)-catalyzed transfer hydrogenations of imines with Hantzsch esters.ORGANIC & BIOMOLECULAR CHEMISTRY,16(9),1448-1451.
MLA Wang, Qiaotian,et al."B(C6F5)(3)-catalyzed transfer hydrogenations of imines with Hantzsch esters".ORGANIC & BIOMOLECULAR CHEMISTRY 16.9(2018):1448-1451.

入库方式: OAI收割

来源:化学研究所

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。