Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water | |
Department | 羰基合成与选择氧化国家重点实验室 |
Chen FX(陈福欣); Shao C(邵成); Liu Q(刘谦); Gong P(龚频); Liu CL(刘春良); Wang R(王锐) | |
2009 | |
Source Publication | Chirality |
ISSN | 0899-0042 |
Volume | 21Pages:600-603 |
Abstract | A mild method for the asymmetric synthesis of quaternary and tertiary carbon centers has been developed through Michael addition of trisubstituted carbon nucleophile to nitroalkenes catalyzed by low loading sodium demethylquinine salt in water. |
Keyword | Organocatalysis Nitroalkenes Quinine Derivate Quaternary Carbon Centers Water |
Subject Area | 物理化学 |
Funding Organization | State Key Laboratory of Applied Organic Chemistry and Institute of Biochemistry and Molecular Biology, Lanzhou University, China, Ministry of Education of China;Natural Science Foundation of China (Contract grant numbers: 20525206;20772052;20621091) |
Indexed By | SCI |
Language | 英语 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.licp.cn/handle/362003/573 |
Collection | 羰基合成与选择氧化国家重点实验室(OSSO) |
Corresponding Author | Wang R(王锐) |
Recommended Citation GB/T 7714 | Chen FX,Shao C,Liu Q,et al. Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water[J]. Chirality,2009,21:600-603. |
APA | 陈福欣,邵成,刘谦,龚频,刘春良,&王锐.(2009).Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water.Chirality,21,600-603. |
MLA | 陈福欣,et al."Asymmetric Michael Addition of Trisubstituted Carbanion to Nitroalkenes Catalyzed by Sodium Demethylquinine Salt in Water".Chirality 21(2009):600-603. |
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