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首页> 外文期刊>RSC Advances >Metal-free n-Et4NBr-catalyzed radical cyclization of disulfides and alkynes leading to benzothiophenes under mild conditions
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Metal-free n-Et4NBr-catalyzed radical cyclization of disulfides and alkynes leading to benzothiophenes under mild conditions

机译:在温和条件下,无金属的n-Et4NBr催化的二硫键和炔烃自由基环化反应生成苯并噻吩

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摘要

A novel n-Et4NBr-catalyzed method for the synthesis of benzothiophene derivatives via cascade reactions of substituted disulfides with alkynes through S-S bond cleavage and alkenyl radical cyclization reactions has been developed. The reaction has a high functional-group tolerance. The new method is environmental and practical, and the starting materials are readily available. These advantages, relative to previous methods, provide an opportunity for the construction of diverse and useful benzothiophene motifs.
机译:开发了一种新颖的n-Et4NBr催化方法,该方法通过取代的二硫键与炔烃通过S-S键断裂和烯基自由基环化反应的级联反应合成苯并噻吩衍生物。该反应具有较高的官能团耐受性。该新方法是环境实用的,并且起始材料容易获得。相对于先前的方法,这些优点为构建各种有用的苯并噻吩基序提供了机会。

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