Department of Chemistry, Indian Institute of Technology Kanpur , Kanpur, UP-208016, India.
Org Lett. 2018 Mar 2;20(5):1320-1323. doi: 10.1021/acs.orglett.8b00053. Epub 2018 Feb 15.
An unusual strategy toward novel substituted benzo[b]thiophenes has been developed. The generation of arynes in the presence of acyl ketene dithioacetals resulted in a cascade reaction involving [3 + 2] cycloaddition, and a dealkylative arylation of a thioether moiety to afford 2,3-disubstuted benzo[b]thiophenes. This route represents an expeditious approach to benzothiophenes that employs acyl ketene dithioacetals as dipoles.
开发了一种新颖的取代苯并[b]噻吩的策略。在酰基烯酮二硫代缩醛存在下生成芳炔,引发了涉及[3 + 2]环加成的级联反应,以及硫醚部分的脱烷基芳基化,生成 2,3-取代的苯并[b]噻吩。该路线代表了一种使用酰基烯酮二硫代缩醛作为偶极子的快速制备苯并噻吩的方法。