An article Photoredox-Catalyzed Addition of Carbamoyl Radicals to Olefins: A 1,4-Dihydropyridine Approach WOS:000539603800001 published article about VISIBLE-LIGHT; ELECTRON; PHOTOEXCITATION; ENERGY; STATE; ACIDS in [Cardinale, Luana; Konev, Mikhail O.; Jacobi von Wangelin, Axel] Univ Hamburg, Dept Chem, Martin Luther King Pl 6, D-20146 Hamburg, Germany in 2020.0, Cited 57.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. COA of Formula: C6H5NO
Functionalization with C1-building blocks are key synthetic methods in organic synthesis. The low reactivity of the most abundant C-1-molecule, carbon dioxide, makes alternative carboxylation reactions with CO2-surrogates especially important. We report a photoredox-catalyzed protocol for alkene carbamoylations. Readily accessible 4-carboxamido-Hantzsch esters serve as convenient starting materials that generate carbamoyl radicals upon visible light-mediated single-electron transfer. Addition to various alkenes proceeded with high levels of regio- and chemoselectivity.
Welcome to talk about 500-22-1, If you have any questions, you can contact Cardinale, L; Konev, MO; von Wangelin, AJ or send Email.. COA of Formula: C6H5NO
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem