Photoredox-Catalyzed Redox-Neutral Minisci C-H Formylation of N-Heteroarenes was written by Dong, Jianyang;Wang, Xiaochen;Song, Hongjian;Liu, Yuxiu;Wang, Qingmin. And the article was included in Advanced Synthesis & Catalysis in 2020.Reference of 36034-54-5 This article mentions the following:
A protocol for redox-neutral Minisci C-H formylation of N-heteroarenes using 1,3-dioxoisoindolin-2-yl 2,2-diethoxyacetate as a formyl equivalent at room temp was reported. This scalable benchtop protocol offered a distinct advantage over traditional reductive carbonylation and Minisci C-H formylation methods in not requiring the use of carbon monoxide, pressurized gas, a stoichiometric reductant, or a stoichiometric oxidant. In the experiment, the researchers used many compounds, for example, 4-Methoxyisoquinoline (cas: 36034-54-5Reference of 36034-54-5).
4-Methoxyisoquinoline (cas: 36034-54-5) belongs to isoquinoline derivatives. Quinoline is a mancude organic heterobicyclic parent, an azaarene, an ortho-fused heteroarene and a member of isoquinolines. They are also used to make oil-soluble dyes, food colorants, pharmaceuticals, pH indicators and other organic compounds. Reference of 36034-54-5
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem