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首页> 外文期刊>Organic & biomolecular chemistry >KHMDS mediated synthesis of 9-arylfluorenes from dibenzothiophene dioxides and arylacetonitriles by tandem S_NAr-decyanation-based arylation
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KHMDS mediated synthesis of 9-arylfluorenes from dibenzothiophene dioxides and arylacetonitriles by tandem S_NAr-decyanation-based arylation

机译:KHMDS介导串联S_NAr-基于脱氰基的芳基化反应由二苯并噻吩二氧化物和芳基乙腈合成9-芳基芴

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摘要

A straightforward KHMDS mediated synthetic route to 9-arylfluorenes from readily available starting materials has been developed. This reaction involves SNAr reactions of dioxide with arylacetonitriles, followed by decyanation reaction. The proposed transformation can also be used to furnish a densely arylated indene.
机译:已经开发了一种简单的由KHMDS介导的从容易获得的起始原料合成9-芳基芴的合成路线。该反应涉及二氧化硫与芳基乙腈的SNAr反应,然后进行脱氰反应。所提出的转化也可以用于提供致密的芳基化的茚。

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  • 来源
    《Organic & biomolecular chemistry》 |2018年第42期|7815-7819|共5页
  • 作者单位

    Cent Univ Rajasthan, Dept Chem, Sch Chem Sci & Pharm, Bandarsindri 305817, Rajasthan, India;

    Cent Univ Rajasthan, Dept Chem, Sch Chem Sci & Pharm, Bandarsindri 305817, Rajasthan, India;

    Cent Univ Rajasthan, Dept Chem, Sch Chem Sci & Pharm, Bandarsindri 305817, Rajasthan, India;

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