首页> 外文会议>日本化学会春季年会講演予稿集 >Methoxylation of Aroyl Fluorides with Cyclopentyl Methyl Ether Mediated by Tetrabutylammonium difluorotriphenylsilicate (TBAT)
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Methoxylation of Aroyl Fluorides with Cyclopentyl Methyl Ether Mediated by Tetrabutylammonium difluorotriphenylsilicate (TBAT)

机译:用四氟甲基二苯基硅基硅酸酯介导的环戊基甲基醚的芳酰氟化物(TBAT)

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The inert bond activation is very useful strategy in modern organic synthesis. The cleavage of carbon-oxygen and carbon-fluorine bond is quite challenging.[1] Many elegant strategies have been developed for C(sp~3)-O bond activation, but these protocols still suffered from being highly dependent on pincer-ligated metal complex, substrates limited to aryl ethers containing a fused aromatic ring or highly nucleophilic triarylphosphines as well as orthodirecting groups.
机译:惰性粘接活化是现代有机合成中的非常有用的策略。碳 - 氧和碳氟键的切割非常具有挑战性。[1]已经开发了许多优雅的策略 - C(SP〜3)-O键活化,但这些方案仍然仍然受到高度依赖于夹持式金属络合物的高度依赖性,基材限于含有稠合的芳环或高亲核三芳基膦的芳基醚正交组。

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