Dipartimento di Chimica, Università degli Studi di Torino, via Pietro Giuria 7, I-10125 Torino, Italy.
J Org Chem. 2021 Jun 18;86(12):8295-8307. doi: 10.1021/acs.joc.1c00746. Epub 2021 Jun 8.
The reactivity of "furan-ynes" in combination with pyridine and quinoline -oxides in the presence of a Au(I) catalyst, has been studied, enabling the synthesis of three different heterocyclic scaffolds. Selective access to two out of the three possible products, a dihydropyridinone and a furan enone, has been achieved through the fine-tuning of the reaction conditions. The reactions proceed smoothly at room temperature and open-air, and were further extended to a broad substrate scope, thus affording functionalized dihydropyridinones and pyranones.
在 Au(I) 催化剂的存在下,研究了“呋喃炔”与吡啶和喹啉氧化物的反应性,从而能够合成三种不同的杂环支架。通过精细调整反应条件,选择性地获得了三种可能产物中的两种,即二氢吡啶酮和呋喃烯酮。反应在室温下和开放空气中顺利进行,并进一步扩展到广泛的底物范围,从而得到了官能化的二氢吡啶酮和吡喃酮。