In 2022,Rio-Rodriguez, Roberto del; Fragoso-Jarillo, Lorena; Garrido-Castro, Alberto F.; Maestro, M. Carmen; Fernandez-Salas, Jose A.; Aleman, Jose published an article in Chemical Science. The title of the article was 《General electrochemical Minisci alkylation of N-heteroarenes with alkyl halides》.Application of 301673-14-3 The author mentioned the following in the article:
A general, facile and environmentally friendly Minisci-type alkylation of N-heteroarenes under simple and straightforward electrochem. conditions using widely available alkyl halides as radical precursors was reported. Primary, secondary and tertiary alkyl radicals were efficiently generated and coupled with a large variety of N-heteroarenes. The method presented a very high functional group tolerance, including various heterocyclic-based natural products, which highlighted the robustness of the method. This applicability was further proved in the synthesis of various interesting biol. valuable building blocks. In addition, a mechanism based on different proofs and pieces of electrochem. evidence was proposed. The results came from multiple reactions, including the reaction of tert-Butyl 4-iodopiperidine-1-carboxylate(cas: 301673-14-3Application of 301673-14-3)
tert-Butyl 4-iodopiperidine-1-carboxylate(cas: 301673-14-3) is one of organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs. Oceanic alkyl iodides are believed to be the principal source of atmospheric iodine.Application of 301673-14-3
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com