Photochemical akynylperfluoroalkylation of unactive alkenes mediated by halogen-bonded charge-transfer complexes†

Huangbin Sun , Chang Huang , Xueting Bin , Fuzhi Cui , Guofang Jiang
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引用次数: 2

Abstract

We describe a catalyst-free visible-light mediated akynylperfluoroalkylation of unactive alkenes with perfluoroalkyl iodides, which provides a series of α-perfluoroalkyl-β-alkynyl ketone derivatives. This new synthetic protocol is enabled by a charge-transfer complex, which is a compound of a 1,4-enynol anion and an enolate ion of acetone as the electron donor and perfluoroalkyl iodides as the electron acceptor. Excellent functional group compatibility and chemoselectivity render this method suitable for fluoroalkylation of pharmaceutically relevant molecules, featuring a broad substrate scope, scalability and significant characteristics of green chemistry, further demonstrating the flexibility and potential for the synthesis of the mentioned compounds.

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卤素键电荷转移配合物介导的非活性烯烃的光化学全氟烷基化反应
我们描述了一种无催化剂可见光介导的非活性烯烃与全氟烷基碘化物的炔基全氟烷基化反应,该反应提供了一系列α-全氟烷基-β-炔基酮衍生物。这种新的合成方案是通过电荷转移络合物实现的,该络合物是1,4-烯醇阴离子和丙酮的烯醇化物离子作为电子供体和全氟烷基碘化物作为电子受体的化合物。优异的官能团兼容性和化学选择性使该方法适用于药物相关分子的氟烷基化,具有广阔的底物范围、可扩展性和显著的绿色化学特征,进一步证明了合成上述化合物的灵活性和潜力。
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Synthesis of biologically active [1,5]diazocino[2,1-b]quinazolinones through [4 + 4] cycloaddition of 2-alkynyl quinazolinones with aza-ortho-quinone methides† Synthesis of fluorinated allylic alcohols via photoinduced decarboxylative cross-coupling of α-fluoroacrylic acids and alcohols† Aromatization-driven cascade [1,5]-hydride transfer/cyclization for synthesis of spirochromanes† Playing with the cavity size of exTTF-based self-assembled cages† An alternative approach to triazatruxene synthesis and derivatization to a boron difluoride complex†
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