A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Formula: C10H24N2, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 4062-60-6, Name is N1,N2-Di-tert-butylethane-1,2-diamine, molecular formula is C10H24N2. In a Article, authors is Bi, Hong-Yan，once mentioned of 4062-60-6
A Tunable Route to Prepare alpha,beta-Unsaturated Esters and alpha,beta-Unsaturated-gamma-Keto Esters through Copper-Catalyzed Coupling of Alkenyl Boronic Acids with Phosphorus Ylides
A tunable strategy to prepare alpha,beta-unsaturated esters and alpha,beta-unsaturated-gamma-keto esters in good to excellent yields was developed through copper-catalyzed oxidative coupling of phosphorus ylides with alkenyl boronic acids under mild conditions. The reaction without water afforded alpha,beta-unsaturated esters, ketones, and amides while alpha,beta-unsaturated-gamma-keto esters, 1,4-alpha,beta-unsaturated diketones and alpha,beta-unsaturated-gamma-keto amides were obtained when using 5.0 equiv. of water. H2O18 labeling experiments showed that water played an important role in the formation of alpha,beta-unsaturated-gamma-keto esters. A plausible formation mechanism for alpha,beta-unsaturated esters and alpha,beta-unsaturated-gamma-keto esters was proposed based on mechanistic studies. Phosphonium salts could also be used directly as coupling partners instead of phosphorus ylides. The reaction exhibited a broad substrate scope, good functional group tolerance, good regioselectivity, and diverse coupling products. (Figure presented.).
I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 4062-60-6, help many people in the next few years.Formula: C10H24N2
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI