Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to beta-Trifluoromethylated Acrylamides
Wen LL(温乐乐) ; Yin L(尹良) ; Shen QL(沈其龙) ; Lv L(吕龙)
刊名ACS Catal.
2013
卷号3期号:4页码:502-506
ISSN号2155-5435
其他题名硝基烷类和其它亲核的β位三氟甲基取代的丙烯酰胺的不对称有机催化迈克尔加成反应
通讯作者沈其龙 ; 吕龙
英文摘要An organocatalytic asymmetric Michael addition of nitroalkanes to trifluoromethylated acrylamides in good yields and with good to excellent diastereoselectivities and excellent enantioselectivities is described. The Michael adducts could be readily transf
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/cs300806w
语种英语
WOS记录号WOS:000317328000003
公开日期2014-10-15
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/29234]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式
GB/T 7714
Wen LL,Yin L,Shen QL,et al. Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to beta-Trifluoromethylated Acrylamides[J]. ACS Catal.,2013,3(4):502-506.
APA 温乐乐,尹良,沈其龙,&吕龙.(2013).Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to beta-Trifluoromethylated Acrylamides.ACS Catal.,3(4),502-506.
MLA 温乐乐,et al."Enantioselective Organocatalytic Michael Addition of Nitroalkanes and Other Nucleophiles to beta-Trifluoromethylated Acrylamides".ACS Catal. 3.4(2013):502-506.
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