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Asymmetric direct alpha-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Bronsted acid via an S(N)1-type pathway
Zhang, Tao1,2; Qiao, Zhen1,2; Wang, Yan1,2; Zhong, Nengjun1,2; Liu, Li1; Wang, Dong1; Chen, Yong-Jun1
刊名CHEMICAL COMMUNICATIONS
2013
卷号49期号:16页码:1636-1638
ISSN号1359-7345
DOI10.1039/c3cc39012h
英文摘要An enantioselective direct alpha-alkylation of 2-oxindoles with Michler's hydrol via an S(N)1-type pathway in the non-covalent activation mode using the bis-cinchona alkaloid and Bronsted acid as a co-catalyst was developed and good to high yields and enantioselectivities were obtained.
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000314187000019
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/54891]  
专题中国科学院化学研究所
通讯作者Liu, Li
作者单位1.Chinese Acad Sci, BNLMS, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Zhang, Tao,Qiao, Zhen,Wang, Yan,et al. Asymmetric direct alpha-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Bronsted acid via an S(N)1-type pathway[J]. CHEMICAL COMMUNICATIONS,2013,49(16):1636-1638.
APA Zhang, Tao.,Qiao, Zhen.,Wang, Yan.,Zhong, Nengjun.,Liu, Li.,...&Chen, Yong-Jun.(2013).Asymmetric direct alpha-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Bronsted acid via an S(N)1-type pathway.CHEMICAL COMMUNICATIONS,49(16),1636-1638.
MLA Zhang, Tao,et al."Asymmetric direct alpha-alkylation of 2-oxindoles with Michler's hydrol catalyzed by bis-cinchona alkaloid-Bronsted acid via an S(N)1-type pathway".CHEMICAL COMMUNICATIONS 49.16(2013):1636-1638.
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