欢迎您!
东篱公司
退出
申报数据库
申报指南
立项数据库
成果数据库
期刊论文
会议论文
著 作
专 利
项目获奖数据库
位置:
成果数据库
>
期刊
> 期刊详情页
Dual Organocatalytic Ion-Pair Assemblies: A Highly Efficient Approach for the Enantioselective Oxa-M
ISSN号:0947-6539
期刊名称:Chemistry-A European Journal
时间:0
页码:801-804
语言:英文
相关项目:离子型手性有机小分子/聚乙二醇复合体系的形成及其催化反应研究
作者:
Tang, Jie|Jiang, Jun-Rong|Luo, Shu-Ping|Xia, Ai-Bao|Xu, Dan-Qian|Wang, Yi-Feng|Xu, Zhen-Yuan|
同期刊论文项目
离子型手性有机小分子/聚乙二醇复合体系的形成及其催化反应研究
期刊论文 29
同项目期刊论文
Complexes of Ionic Liquids with Poly(ethylene glycol)s
Enantioselective Michael Addition of Aromatic Ketones to Nitroolefins Catalyzed by Bifunctional Thio
Chiral Squaramides as Highly Enantioselective Catalysts for Michael Addition Reactions of 4-Hydroxyc
The highly enantioselective Michael addition of ketones to nitrodienes catalyzed by the efficient or
Highly Enantioselective Organocatalytic Michael Addition of 2-Hydroxy-1,4-naphthoquinone to beta,gam
An Organocatalytic Domino Thia-Michael/Aldol Condensation Reaction: Highly Enantioselective Synthesi
(1R,2R)-N,N'-Bis(ferrocenylmethyl)-1,2-diphenylethane-1,2-diamine
(R)-2-(2-Methoxyphenyl)-2,5-dihydrothiophene-3-carbaldehyde
(4R)-Ethyl 4-(4-chlorophenyl)-2-hydroxy-5-oxo-2,3,4,5-tetrahydropyrano[3,2-c]chrome ne-2-carboxylate
Ethyl (2S,4R)-4-(4-bromophenyl)-2-hydroxy-5,10-dioxo-3,4,5,10-tetrahydro-2H-be nzo[g]chromene-2-carb
2-1(imidazolylthio)methyllpyrrolidine as a trifunctional organocatalyst for the highly asymmetric Mi
A Novel Enantioselective Catalytic Tandem Oxa-Michael-Henry Reaction: One-Pot Organocatalytic Asymme
(S)-2-[(2-ammoniophenyl)sulfanylmethyl]pyrrolidinium dibromide
(S)-2-(pyrrolidinium-2-ylmethylsulfanyl)pyridinium dibromide
(S)-1-(2-ammonio-3-methylbutyl)-1,2-dihydropyridin-2-iminiumdibromide
1-[3,5-bis(trifluoromethyl)phenyl]-3-(2-pyridyl)thiourea
(S)-2-Amino-1-(pyrrolidinium-2-ylmethyl)pyridinium dibromide
A chiral thioureido acid as an effective additive for enantioselective organocatalytic Michael addit
One-Pot Organocatalytic Asymmetric Synthesis of 3-Nitro-1,2-dihydroquinolines by a Dual-Activation P
Chiral amine/chiral acid as an excellent organocatalytic system for the enantioselective tandem oxa-
(S)-3-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]thian-4-one
(2R,5S)-5-Benzyl-2,3-dimethyl-4-oxo-2-phenylimidazolidin-1-ium chloride
(1S,4S,5S,6R)-6-(4-Bromophenyl)-5-nitrobicyclo[2.2.2]octan-2-one
In Situ Enamine Activation in Aqueous Salt Solutions: Highly Efficient Asymmetric Organocatalytic Di
(2R,4R)-2-Hydroxy-4-(2-methoxyphenyl)bicyclo[3.3.1]nonan-9-one
(R)-7-Bromo-2,3,4,4a-tetrahydro-1H-xanthen-1-one
(S)-2-[(S,E)-4-(4-Chlorophenyl)-1-nitrobut-3-en-2-yl]cyclohexanone
Ethyl 2-hydroxy-5-oxo-4-phenyl-2,3,4,5-tetrahydropyrano[3,2-c]chromene-2-carbo xylate