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双环丁烷与硫酮的(3 + 2)环加成反应:无需使用催化剂或光照即可合成2-硫杂双环[2.1.1]己烷

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

作者信息

Knyazev Daniil A, George Malini, Werz Daniel B

机构信息

Albert-Ludwigs-Universität Freiburg, Institute of Organic Chemistry Albertstr. 21 79104 Freiburg Germany

出版信息

Chem Sci. 2025 Apr 2;16(19):8588-8593. doi: 10.1039/d5sc00125k. eCollection 2025 May 14.

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.

摘要

一种合成2-硫杂双环[2.1.1]己烷骨架的新方法已被报道。该方法利用了两种高活性物种:双环[1.1.0]丁烷(BCBs)和硫酮。它们的高反应活性使得所需产物在环境条件下即可形成,无需催化剂、添加剂或光照。据我们所知,这是首次对这种特定骨架进行合理合成。研究了各种羰基取代的BCBs,其桥头的另一侧有或没有取代基,以及硫酮。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc90/12077308/4ca28912feff/d5sc00125k-s1.jpg

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