Wang Jie, Zheng Mingyue, Jia Qianfa, Ren Qiao, Wu Jicheng
Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, Innovative Drug Research Center, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, P. R. China.
Chongqing Key Laboratory for New Chemical Materials of Shale Gas, College of Chemistry and Chemical Engineering, Yangtze Normal University, Chongqing 408100, P. R. China.
Org Lett. 2024 Jun 14;26(23):4868-4872. doi: 10.1021/acs.orglett.4c01253. Epub 2024 Jun 4.
A new strategy for facile access to multifunctionalized furans via -heterocyclic carbene-catalyzed cross-coupling/cyclization of ynenones with aldehydes has been explored. This protocol features readily obtainable starting materials, mild and metal-free conditions, broad substrate scope, good functional group tolerance, excellent yields, and easy scale-up. Synthetic utility of the protocol has been further corroborated through functionalization of complex substrates and postmodifications of the product.
通过-杂环卡宾催化的烯炔酮与醛的交叉偶联/环化反应,开发了一种简便合成多官能化呋喃的新策略。该方法具有起始原料易于获得、条件温和且无金属、底物范围广、官能团耐受性好、产率高以及易于放大等特点。通过复杂底物的官能化和产物的后期修饰,进一步证实了该方法的合成实用性。