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Deconstructing the Catalytic, Vicinal Difluorination of Alkenes: HF-Free Synthesis and Structural Study of p-TolIF(2)

机译:解构催化,邻烷基的邻甲基二氟:P-Tolif的无酸合成和结构研究(2)

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摘要

Recently, contemporaneous strategies to achieve the vicinal difluorination of alkenes via an I(I)/I(III) catalysis manifold were independently reported by this laboratory and by Jacobsen and co-workers. Both strategies proceed through a transient ArI(III)F-2 species generated by oxidation of the An catalyst. Herein, an efficient synthesis of p-TolIF(2) from p-Toll and Selectfluor is presented, together with a crystallographic and spectroscopic study. To mitigate safety concerns and simplify reaction execution, an HF-free protocol was devised employing CsF as a substitute fluoride source. The study provides insight into the initial I(I)-> I(III) oxidation stage of the catalytic protocol using Selectfluor.
机译:最近,通过I(i)/ i(III)催化歧管的同时策略达到烯烃的烯烃二氟化,由该实验室和Jacobsen和Co-Workers独立地报道。 两种策略通过催化剂氧化产生的瞬态ARI(III)F-2物种。 这里,呈现来自P-Toll和Selectfluor的P-Tolif(2)的有效合成,以及结晶和光谱研究。 为了减轻安全问题并简化反应执行,设计了一种HF的方案,用于使用CSF作为替代氟化物来源。 该研究提供了使用Selectfluor对催化方案的初始I(I) - > I(III)氧化阶段的洞察。

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  • 来源
    《The Journal of Organic Chemistry》 |2017年第22期|共7页
  • 作者单位

    Westfal Wilhelms Univ Munster Inst Organ Chem Corrensstr 40 D-48149 Munster Germany;

    Westfal Wilhelms Univ Munster Inst Organ Chem Corrensstr 40 D-48149 Munster Germany;

    Westfal Wilhelms Univ Munster Inst Organ Chem Corrensstr 40 D-48149 Munster Germany;

    Westfal Wilhelms Univ Munster Inst Organ Chem Corrensstr 40 D-48149 Munster Germany;

    Westfal Wilhelms Univ Munster Inst Organ Chem Corrensstr 40 D-48149 Munster Germany;

    Westfal Wilhelms Univ Munster Inst Organ Chem Corrensstr 40 D-48149 Munster Germany;

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  • 正文语种 eng
  • 中图分类 有机化学;
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