中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Organocatalyzed aza-Michael-Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers

文献类型:期刊论文

作者Huang YM(黄有銘) ; Zheng CW(郑昌武) ; Zhao G(赵刚)
刊名RSC Adv.
出版日期2013
卷号3期号:38页码:16999-17002
ISSN号2046-2069
其他题名有机催化氮杂迈克尔-迈克尔串联反应构筑具有全碳手性中心氧化吲哚-四氢喹啉
通讯作者赵刚
英文摘要An efficient organocatalytic aza-Michael-Michael cascade reaction for the asymmetric synthesis of highly functionalized spirooxindole tetrahydroquinolines has been reported through a formal [4+2] annulation strategy.
学科主题天然产物有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c3ra42783h
语种英语
WOS记录号WOS:000325272100018
公开日期2014-10-15
源URL[http://ir.sioc.ac.cn/handle/331003/29256]  
专题上海有机化学研究所_中科院天然产物有机化学重点实验室
推荐引用方式
GB/T 7714
Huang YM,Zheng CW,Zhao G. Organocatalyzed aza-Michael-Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers[J]. RSC Adv.,2013,3(38):16999-17002.
APA 黄有銘,郑昌武,&赵刚.(2013).Organocatalyzed aza-Michael-Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers.RSC Adv.,3(38),16999-17002.
MLA 黄有銘,et al."Organocatalyzed aza-Michael-Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers".RSC Adv. 3.38(2013):16999-17002.

入库方式: OAI收割

来源:上海有机化学研究所

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