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首页> 外文期刊>Tetrahedron >Electrophilic substitution reactions of trisheteroarylinethanes: an efficient strategy to develop novel synthons for organic synthesis
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Electrophilic substitution reactions of trisheteroarylinethanes: an efficient strategy to develop novel synthons for organic synthesis

机译:三杂芳基乙烷的亲电取代反应:开发用于有机合成的新型合成子的有效策略

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摘要

Trisheteroarylmethanes are interesting molecules for the construction of three dimensionally complex systems. From this vantage point, we studied electrophilic substitution reactions on tris-2-thienylmethane and tris-2-furylmethane. During the bromination reaction, we have isolated the tris-bromosubstituted tris-2-thienylmethane in the former case and brominated furanones in the latter case, which may be of synthetic and biological importance. (c) 2005 Elsevier Ltd. All rights reserved.
机译:三硬脂基甲烷是构建三维复杂系统的有趣分子。从这个有利的角度出发,我们研究了在Tris-2-噻吩基甲烷和Tris-2-呋喃基甲烷上的亲电取代反应。在溴化反应过程中,前者分离出了三溴取代的三-2-噻吩基甲烷,后者分离出了呋喃呋喃酮,这可能具有合成和生物学意义。 (c)2005 Elsevier Ltd.保留所有权利。

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