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学科主题: 氟化学
题名: Nucleophilic difluoro(phenylsulfonyl)methylation of carbonyls with PhSO2CF2H reagent in the presence of in situ generated substoichiometric amount of base
其他题名: 现场产生的亚化学计量的碱所促进的二氟甲基苯基砜(PhSO2CF2H)与羰基化合物的加成反应
作者: Hu MY(胡明友) ; Gao B(高兵) ; Ni CF(倪传法) ; Zhang LJ(张来俊) ; Hu JB(胡金波)
通讯作者: 胡金波
刊名: J. Fluor. Chem.
发表日期: 2013
卷: 155, 页:52-58
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所, 有机氟化学重点实验室
英文摘要: The reactions between carbonyl compounds and PhSO2CF2H using substoichiometric amount of base in situ generated from N(TMS)(3) and catalytic amount of Me4NF have been investigated. It is found that both enolizable and non-enolizable aldehydes are suitable
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000325447900006
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/29205
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:
Hu MY,Gao B,Ni CF,et al. Nucleophilic difluoro(phenylsulfonyl)methylation of carbonyls with PhSO2CF2H reagent in the presence of in situ generated substoichiometric amount of base[J]. J. Fluor. Chem.,2013,155:52-58.
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