Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences , Tohoku University , 6-3 Aoba, Aramaki, Aoba-ku , Sendai 980-8578 , Japan.
Org Lett. 2018 Oct 5;20(19):6104-6107. doi: 10.1021/acs.orglett.8b02528. Epub 2018 Sep 18.
The chemoselective oxidation of alcohols containing electron-rich sulfur functionalities (e.g., 1,3-dithianes and sulfides) into their corresponding carbonyl compounds with the sulfur groups can sometimes be a demanding task in modern organic chemistry. A reliable method for this transformation, which features azaadamantane-type nitroxyl radical/copper catalysis using ambient air as the terminal oxidant is reported. The superiority of the developed method was demonstrated by comparing it with various conventional alcohol oxidation methods.
含有富电子硫官能团(例如 1,3-二噻烷和硫醚)的醇的化学选择性氧化成相应的羰基化合物,其中硫基团可以在现代有机化学中有时是一项艰巨的任务。本文报道了一种使用氮氧自由基/铜催化,以环境空气为末端氧化剂的可靠方法。通过与各种传统的醇氧化方法进行比较,证明了所开发方法的优越性。