黄素组
化学
硫脲
催化作用
电化学
背景(考古学)
光化学
酒精氧化
组合化学
酒
小学(天文学)
范围(计算机科学)
电解
氧化还原
有机化学
电催化剂
苯甲醇
反应机理
激进的
反应条件
反应中间体
伯醇
降级(电信)
氧化还原
光催化
作者
Wen Zhang,Keith L. Carpenter,Song Lin
标识
DOI:10.1002/anie.201910300
摘要
Abstract Riboflavin‐derived photocatalysts have been extensively studied in the context of alcohol oxidation. However, to date, the scope of this catalytic methodology has been limited to benzyl alcohols. In this work, mechanistic understanding of flavin‐catalyzed oxidation reactions, in either the absence or presence of thiourea as a cocatalyst, was obtained. The mechanistic insights enabled development of an electrochemically driven photochemical oxidation of primary and secondary aliphatic alcohols using a pair of flavin and dialkylthiourea catalysts. Electrochemistry makes it possible to avoid using O 2 and an oxidant and generating H 2 O 2 as a byproduct, both of which oxidatively degrade thiourea under the reaction conditions. This modification unlocks a new mechanistic pathway in which the oxidation of unactivated alcohols is achieved by thiyl radical mediated hydrogen‐atom abstraction.
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