Guzman Alexander L, Kevorkian Paul V, Hoye Thomas R
Department of Chemistry, University of Minnesota, 207 Pleasant Street Southeast, Minneapolis, Minnesota 55455, United States.
Org Lett. 2024 May 10;26(18):3834-3839. doi: 10.1021/acs.orglett.4c01005. Epub 2024 Apr 30.
2:1 adducts arise from the reaction of 2,5-diaryl-1,3,4-oxadiazoles and benzynes generated from the hexadehydro-Diels-Alder (HDDA) reaction. Density functional theory computations support a mechanistic manifold that includes a concerted SAr process. Additionally, the benzyne trapping reaction of 2,5-dimethyl-1,3,4-oxadiazole affords an unusual acylimine-containing 2:1 adduct, which is the first case in which a dearomatized product has arisen from a HDDA reaction.
2:1加合物由2,5-二芳基-1,3,4-恶二唑与通过六脱氢狄尔斯-阿尔德(HDDA)反应生成的苯炔反应产生。密度泛函理论计算支持一个包括协同亲核芳环取代过程的机理体系。此外,2,5-二甲基-1,3,4-恶二唑的苯炔捕获反应得到一种不同寻常的含酰亚胺2:1加合物,这是首次出现通过HDDA反应生成去芳构化产物的情况。