中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent

文献类型:期刊论文

作者Lv GH ; Jin RH ; Mai WP ; Gao LX
刊名tetrahedron-asymmetry
出版日期2008
卷号19期号:22页码:2568-2572
关键词CHIRAL IONIC LIQUID DIELS-ALDER REACTIONS ALDOL REACTION RECYCLABLE ORGANOCATALYST SUPPORTED ORGANOCATALYST L-PROLINE PYRROLIDINE SULFONAMIDE ENANTIOSELECTIVE ALDOL WATER ALDEHYDES
ISSN号0957-4166
通讯作者gao lx
中文摘要a series of pyrrolidine-triazole based dendritic catalysts have been synthesized and applied directly in the asymmetric michael addition of ketones to nitroolefins without the use of an organic solvent. good yields (up to 99%), and high diastereoselectivities (up to syn/anti = 45:1) and enantioselectivities (up to 95% ee) have been obtained. furthermore. the third generation catalyst can be reused at least five times without significant loss of catalytic activity. (c) 2008 elsevier ltd. all rights reserved.
收录类别SCI
语种英语
WOS记录号WOS:000262053900017
公开日期2010-04-14
源URL[http://ir.ciac.jl.cn/handle/322003/10785]  
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
Lv GH,Jin RH,Mai WP,et al. Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent[J]. tetrahedron-asymmetry,2008,19(22):2568-2572.
APA Lv GH,Jin RH,Mai WP,&Gao LX.(2008).Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent.tetrahedron-asymmetry,19(22),2568-2572.
MLA Lv GH,et al."Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent".tetrahedron-asymmetry 19.22(2008):2568-2572.

入库方式: OAI收割

来源:长春应用化学研究所

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。