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Organocatalytic enantioselective alpha-amination of 5-substituted rhodanines: an efficient approach to chiral N,S-acetals
Zhang, Huanrui; Wang, Baomin; Cui, Longchen; Li, Ying; Qu, Jingping; Song, Yuming
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
2014
卷号12页码:9097-9100
ISSN号1477-0520
URL标识查看原文
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/4425801
专题大连理工大学
作者单位Dalian Univ Technol, Sch Pharmaceut Sci & Technol, State Key Lab Fine Chem, Dalian 116024, Peoples R China.
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GB/T 7714
Zhang, Huanrui,Wang, Baomin,Cui, Longchen,et al. Organocatalytic enantioselective alpha-amination of 5-substituted rhodanines: an efficient approach to chiral N,S-acetals[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2014,12:9097-9100.
APA Zhang, Huanrui,Wang, Baomin,Cui, Longchen,Li, Ying,Qu, Jingping,&Song, Yuming.(2014).Organocatalytic enantioselective alpha-amination of 5-substituted rhodanines: an efficient approach to chiral N,S-acetals.ORGANIC & BIOMOLECULAR CHEMISTRY,12,9097-9100.
MLA Zhang, Huanrui,et al."Organocatalytic enantioselective alpha-amination of 5-substituted rhodanines: an efficient approach to chiral N,S-acetals".ORGANIC & BIOMOLECULAR CHEMISTRY 12(2014):9097-9100.
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