Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
Department of Chemistry, University of California─Davis, Davis, California 95616, United States.
J Org Chem. 2022 Jul 15;87(14):8983-9000. doi: 10.1021/acs.joc.2c00696. Epub 2022 Jun 25.
A variety of Huisgen cyclization or nitrene/carbene alkyne cascade reactions with different types of termination were investigated. Accessible nitrene precursors were assessed, and carbonazidates were found to be the only effective initiators. Solvents, terminal alkynyl substituents, and catalysts can all impact the reaction outcome. Study of the mechanism both computationally (by density functional theory) and experimentally revealed relevant intermediates and plausible reaction pathways.
研究了多种不同类型的 Huisgen 环化或氮烯/卡宾炔烃级联反应。评估了可及的氮烯前体,发现碳氮宾是唯一有效的引发剂。溶剂、末端炔基取代基和催化剂都可以影响反应结果。通过密度泛函理论(DFT)计算和实验研究揭示了相关中间体和可能的反应途径。