Issue 19, 2025

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

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.

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

Supplementary files

Article information

Article type
Edge Article
Submitted
07 Янв. 2025
Accepted
02 Апр. 2025
First published
02 Апр. 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2025,16, 8588-8593

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

D. A. Knyazev, M. George and D. B. Werz, Chem. Sci., 2025, 16, 8588 DOI: 10.1039/D5SC00125K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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