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首页> 外文期刊>Organic & biomolecular chemistry >Triflic acid-promoted cycloisomerization of 2-alkynylphenyl isothiocyanates and isocyanates: a novel synthetic method for a variety of indole derivatives
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Triflic acid-promoted cycloisomerization of 2-alkynylphenyl isothiocyanates and isocyanates: a novel synthetic method for a variety of indole derivatives

机译:Triflic酸促进的2-炔基苯基异硫氰酸酯和异氰酸酯的环异构化:多种吲哚衍生物的新颖合成方法

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摘要

A new approach towards the synthesis of indole derivatives via triflic acid-promoted cycloisomerization with rearrangement of 2-(alkyn-1-yl)phenyl isothiocyanates and 2-(alkyn-1-yl)phenyl isocyanates has been achieved. By this methodology, structurally diverse types of indole derivatives such as thieno- and furo-indoles, spiro-indolethiones, spiro-oxindoles, and 3-alkylidene-oxindoles were synthesized.
机译:已经实现了通过三氟甲磺酸促进的环异构化并重排2-(炔-1-基)苯基异硫氰酸酯和2-(炔-1-基)苯基异氰酸酯来合成吲哚衍生物的新方法。通过这种方法,合成了结构上不同类型的吲哚衍生物,如噻吩-和呋喃-吲哚,螺-吲哚硫酮,螺-羟吲哚和3-亚烷基-氧吲哚。

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  • 来源
    《Organic & biomolecular chemistry》 |2014年第42期|8398-8407|共10页
  • 作者单位

    Department of Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan;

    Department of Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan;

    Department of Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan;

    Department of Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan,International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577, Japan;

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