School of Chemistry and Materials Science Key Laboratory of Chemical Engineering Process & Technology for High-efficiency Conversion, Heilongjiang University, Harbin, 150080, P. R. China.
Chem Asian J. 2020 Jul 1;15(13):1976-1981. doi: 10.1002/asia.202000277. Epub 2020 May 27.
A visible light-induced decarboxylative alkylation of heterocyclic aromatics with aliphatic carboxylic acids was developed by using anthocyanins as a photocatalyst under mild conditions. A series of alkylated heterocyclic compounds were obtained in moderate to good yields by using the metal-free decarboxylative coupling reaction under blue light. This strategy uses cheap and readily available carboxylic acids as alkylation reagents with good functional group tolerance and environmental friendliness. It is worth noting that this is the first time that anthocyanin has been used to catalyze the Minisci-type C-H alkylation. The mechanism of decarboxylation alkylation was studied by capturing the adduct of alkyl radical and hydroquinone, thus confirming a radical mechanism. This protocol provides an alternative visible light-induced decarboxylative alkylation for the functionalization of heterocyclic aromatics.
可见光诱导的杂环芳烃与脂肪族羧酸的脱羧烷基化反应,在温和条件下,以花青素作为光催化剂得以发展。通过使用无金属的脱羧偶联反应,在蓝光下可以中等至良好的收率得到一系列烷基化杂环化合物。该策略使用廉价易得的羧酸作为烷基化试剂,具有良好的官能团容忍性和环境友好性。值得注意的是,这是花青素首次被用于催化 Minisci 型 C-H 烷基化反应。通过捕获烷基自由基和对苯二酚的加合物,研究了脱羧烷基化的反应机理,从而证实了自由基机理。该方案为杂环芳烃的功能化提供了一种可见光诱导的脱羧烷基化的替代方法。