Mindner Jasper, Rombach Sina, Werz Daniel B
Institute of Organic Chemistry, Albert-Ludwigs-Universität Freiburg, Albertstrasse 21, 79104 Freiburg im Breisgau, Germany.
Org Lett. 2024 Mar 15;26(10):2124-2128. doi: 10.1021/acs.orglett.4c00498. Epub 2024 Mar 1.
In this report, we describe the multicomponent coupling reaction between arynes, (pseudo)halides, and an electrophilic chalcogen species. Addition of a copper salt enabled smooth conversion by suppressing side reactions. A variety of different aryne precursors as well as seleno- and thiosulfonates were employed, yielding a broad spectrum of -(pseudo)halogenated chalcogenides. This motif was subjected to different cross-coupling approaches, demonstrating the applicability of these compounds as building blocks for more complex structures.
在本报告中,我们描述了芳炔、(拟)卤化物和亲电硫属元素物种之间的多组分偶联反应。加入铜盐可通过抑制副反应实现顺利转化。使用了多种不同的芳炔前体以及硒代磺酸盐和硫代磺酸盐,得到了广泛的一系列(拟)卤代硫属元素化物。该反应模式采用了不同的交叉偶联方法,证明了这些化合物作为构建更复杂结构的基石的适用性。