(3 + 2)-Cycloaddition of bicyclobutanes and thioketones: access to 2-thiabicyclo[2.1.1]hexanes without the use of catalysts or light†

IF 7.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Chemical Science Pub Date : 2025-04-02 DOI:10.1039/D5SC00125K
Daniil A. Knyazev, Malini George and Daniel B. Werz
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Abstract

A novel approach to the synthesis of a 2-thiabicyclo[2.1.1]hexane scaffold has been described. This method utilizes two highly reactive species: bicyclo[1.1.0]butanes (BCBs) and thioketones. Their high reactivity enabled the formation of the desired product to occur under ambient conditions, without the need for catalysts, additives or light irradiation. To the best of our knowledge, this is the first rational synthesis of this specific skeleton. A variety of carbonyl-substituted BCBs, with or without a substituent at the other bridgehead, and thioketones were examined.

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(3+2)-双环丁烷和硫酮的环加成:在不使用催化剂或光的情况下获得2-硫代双环[2.1.1]己烷
介绍了一种合成2-硫代双环[2.1.1]己烷支架的新方法。该方法利用了两种高活性物质:自行车[1.1.0]丁烷(BCBs)和硫酮。它们的高反应性使所需产物的形成在环境条件下发生,不需要催化剂、添加剂或光照射。据我们所知,这是这种特殊骨骼的第一次合理合成。研究了各种羰基取代的bcb,在桥头堡上有或没有取代基,以及硫酮。
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来源期刊
Chemical Science
Chemical Science CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
4.80%
发文量
1352
审稿时长
2.1 months
期刊介绍: Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.
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