Cinchona alkaloid thiourea mediated asymmetric Mannich reaction of isocyanoacetates with isatin-derived ketimines and subsequent cyclization: enantioselective synthesis of spirooxindole imidazolines
Zhao, Mei-Xin1,2,3; Jing, Lei1,2; Zhou, Hao1,2; Shi, Min1,2,4
刊名RSC ADVANCES
2015
卷号5期号:92页码:75648-75652
英文摘要We report the organocatalyzed asymmetric Mannich reaction of isocyanoacetates with isatin derived ketimines in good yields along with high stereoselectivities. The subsequent organocatalyzed cyclization of Mannich adducts is also investigated, emerging as a promising strategy for the synthesis of optically active spirooxindole imidazolines.
收录类别SCI
语种英语
公开日期2015-11-03
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/28395]  
专题化学研究所_分子识别与功能实验室
作者单位1.E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
2.E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China
3.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
4.Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
推荐引用方式
GB/T 7714
Zhao, Mei-Xin,Jing, Lei,Zhou, Hao,et al. Cinchona alkaloid thiourea mediated asymmetric Mannich reaction of isocyanoacetates with isatin-derived ketimines and subsequent cyclization: enantioselective synthesis of spirooxindole imidazolines[J]. RSC ADVANCES,2015,5(92):75648-75652.
APA Zhao, Mei-Xin,Jing, Lei,Zhou, Hao,&Shi, Min.(2015).Cinchona alkaloid thiourea mediated asymmetric Mannich reaction of isocyanoacetates with isatin-derived ketimines and subsequent cyclization: enantioselective synthesis of spirooxindole imidazolines.RSC ADVANCES,5(92),75648-75652.
MLA Zhao, Mei-Xin,et al."Cinchona alkaloid thiourea mediated asymmetric Mannich reaction of isocyanoacetates with isatin-derived ketimines and subsequent cyclization: enantioselective synthesis of spirooxindole imidazolines".RSC ADVANCES 5.92(2015):75648-75652.
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