中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Metal-Mediated Reformatsky Reaction of Bromodifluoromethyl Ketone and Imine

文献类型:期刊论文

作者Cao CR(曹春如); Jiang M(蒋敏); Liu JT(刘金涛)
刊名Eur. J. Org. Chem.
出版日期2015
期号5页码:1144-1151
其他题名金属促进的溴二氟甲基酮和亚胺的Reformatsky反应
通讯作者刘金涛
英文摘要The Reformatsky reaction of bromodifluoromethyl ketones and imines took place readily in the presence of Zn/CuCl at room temperature to afford beta-amino alpha,alpha-difluoro ketones in good yields. Using (S)-tert-butanesulfinyl as a chiral auxiliary, the asymmetric Reformatsky reaction was also achieved and found to proceed with excellent diastereoselectivities. A plausible model is proposed to account for the high stereoselectivity of the reaction.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/ejoc.201403424
语种英语
WOS记录号WOS:000349391700028
源URL[http://ir.sioc.ac.cn/handle/331003/39704]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
作者单位中科院上海有机化学研究所, 有机氟化学重点实验室
推荐引用方式
GB/T 7714
Cao CR,Jiang M,Liu JT. Metal-Mediated Reformatsky Reaction of Bromodifluoromethyl Ketone and Imine[J]. Eur. J. Org. Chem.,2015(5):1144-1151.
APA 曹春如,蒋敏,&刘金涛.(2015).Metal-Mediated Reformatsky Reaction of Bromodifluoromethyl Ketone and Imine.Eur. J. Org. Chem.(5),1144-1151.
MLA 曹春如,et al."Metal-Mediated Reformatsky Reaction of Bromodifluoromethyl Ketone and Imine".Eur. J. Org. Chem. .5(2015):1144-1151.

入库方式: OAI收割

来源:上海有机化学研究所

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