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学科主题: 氟化学
题名: Enantioselective Organocatalytic Michael Addition of Aldehydes to Trifluoroethylidene Malonates
其他题名: Enantioselective Organocatalytic Michael Addition of Aldehydes to Trifluoroethylidene Malonates
作者: Wen LL(温乐乐) ; Shen QL(沈其龙) ; Lv L(吕龙)
通讯作者: 吕龙
刊名: Org. Lett.
发表日期: 2010
卷: 12, 期:20, 页:4655-4657
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所
英文摘要: An efficient, highly enantioselective, organocatalytic Michael addition reaction of aldehydes with trilluoroethylidene malonates is described The asymmetric reaction provided highly optically pure beta-trifluoromethyl aldehydes which can be conveniently transformed into 4,4,4-trifluoromethyl butyric acid and trifluoromethyl substituted delta-lactones without loss in enantioselectivity
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000282604700057
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/19227
Appears in Collections:中科院有机氟化学重点实验室_期刊论文

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Recommended Citation:
Wen LL,Shen QL,Lv L. Enantioselective Organocatalytic Michael Addition of Aldehydes to Trifluoroethylidene Malonates[J]. Org. Lett.,2010,12(20):4655-4657.
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