Product Details of 123-11-5. Recently I am researching about STEREOSELECTIVE-SYNTHESIS; SYNTHETIC APPLICATIONS; ALPHA-CHLOROESTERS; CARBOLITHIATION; HALIDES, Saw an article supported by the European France-(Manche)England cross-border cooperation program INTERREG V A LABFACT; ERDFEuropean Commission; Normandie Universite; CNRSCentre National de la Recherche Scientifique (CNRS)European Commission; INSA Rouen; Carnot I2C; LabEx SynOrg [ANR-11-LABX-0029]; Region NormandieRegion Normandie. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Dejardin, C; Renou, A; Maddaluno, J; Durandetti, M. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde
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.
Product Details of 123-11-5. 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