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首页> 外文期刊>The Journal of Organic Chemistry >In situ generation of 3,3,3-trifluoropropanal and its use for carbon-carbon bond-forming reactions
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In situ generation of 3,3,3-trifluoropropanal and its use for carbon-carbon bond-forming reactions

机译:3,3,3-三氟丙醛的原位生成及其在碳-碳键形成反应中的应用

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摘要

The DIBAL reduction of 2-phenylethyl 3,3,3-trifluoro-2-methylpropionate 2 at -78 degrees C afforded the aluminum acetal 3, and this intermediate, on Worming Lip to 0 T, Was found to slowly decompose into the corresponding aldehyde 4, which smoothly reacted with appropriate nucleophiles in a one-pot manner in good to excellent yields with Lip to 93% diastereoselectivity.
机译:在-78℃下将2-苯基乙基3,3,3-三氟-2-甲基丙酸酯2进行DIBAL还原,得到缩醛铝3,发现该中间体在Worming Lip上降至0 T,缓慢分解为相应的醛4,其与合适的亲核试剂以一锅法顺利反应,具有良好或优异的产率,Lip达到93%的非对映选择性。

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