Nucleophilic Difluoromethylenation of Aldehydes and Ketones Using diethyl(difluoro(trimethylsilyl)me

来源 :中国化学会全国第十二届有机合成化学学术研讨会 | 被引量 : 0次 | 上传用户：yy19880904

【摘要】

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【作者】

：

Wang Yu-Hui Zhou Jian

【机构】

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Shanghai Key Laboratory of Green Chemistry and Chemical Processes,School of Chemistry and Molecular

【出处】

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中国化学会全国第十二届有机合成化学学术研讨会

【发表日期】

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2015年7期

【关键词】

：

Difluoromethylenation Nucleophilic addition

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　　Fluorine is either an isoelectronic replacement for the hydroxyl group or a bioisosteric replacement for hydrogen,affecting metabolic degradation,lipophilicity,hydrogen bonding,and reactivity of organic molecules.The chemistry of fluorinated alkylphosphonates may help to study the possible effect of such substitution on physical,chemical,and biological properties of the resulting phosphonates.1,2 Herein,a new nucleophilic difluoromethylenation of aldehydes and ketones using diethyl(difluoro(trimethylsilyl)methyl)phosphonate 1 has been achieved.

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Nucleophilic Difluoromethylenation of Aldehydes and Ketones Using diethyl(difluoro(trimethylsilyl)me

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