Kim Han Byeol, Han Dong Kyun, Lee Jae Kyun, Han Seo-Jung
Department of Chemistry, Sogang University 35 Baekbeom Ro Seoul 04107 Republic of Korea
Center for Nano Materials, Sogang University 35 Baekbeom Ro Seoul 04107 Republic of Korea.
RSC Adv. 2025 May 15;15(21):16276-16280. doi: 10.1039/d5ra02693h.
We reported a metal-free electrochemical oxidative C-O homocoupling of 2-naphthols, followed by subsequent alkoxylation under mild conditions. This strategy offered an eco-friendly and cost-effective electrochemical approach using undivided cells. Additionally, the reaction exhibited broad tolerance to various substituted 2-naphthols and diverse alcohols, affording the corresponding naphthalenones in moderate to good yields.
我们报道了一种无金属的2-萘酚电化学氧化C-O均偶联反应,随后在温和条件下进行烷氧基化反应。该策略提供了一种使用无隔膜电池的环保且经济高效的电化学方法。此外,该反应对各种取代的2-萘酚和不同的醇类表现出广泛的耐受性,以中等至良好的产率得到相应的萘醌。