Dejardin, C; Renou, A; Maddaluno, J; Durandetti, M in [Dejardin, Claire; Renou, Amaury; Maddaluno, Jacques; Durandetti, Muriel] Normandie Univ, UNIROUEN, INSA Rouen, CNRS,Lab COBRA UMR 6014 & FR 3038, F-76000 Rouen, France published Nickel-Catalyzed Electrochemical Cyclization of Alkynyl Aryl Iodide and the Domino Reaction with Aldehydes in 2021, Cited 42. Recommanded Product: 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.
An intramolecular carbometallation of a triple bond promoted by electrochemistry and mediated by nickel catalysis is described. This domino process transforms various aryl halides bearing a propargyl chain into substituted heterocycles in one single operation, with high stereoselectivities and in good to high yields. This reaction, characterized by a cyclic voltammetry set of experiments, proceeds following a syn-exo-dig cyclization process. When run at 80 degrees C, vinylbenzofuranes that are suitable substrates for cycloaddition reactions are obtained.
Recommanded Product: 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Dejardin, C; Renou, A; Maddaluno, J; Durandetti, M or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles