An article Palladium-Catalyzed Decarboxylative Generation and Propargylation of 2-Azaallyl Anions WOS:000475459200017 published article about SUPER-ELECTRON-DONORS; COUPLING REACTION; DOUBLE-BLIND; REGIOSELECTIVITY; VIRIDENOMYCIN; DERIVATIVES; CARBONATES in [Tang, Shaojian; Wei, Wenjing; Yin, Dan; Poznik, Michal; Chruma, Jason J.] Sichuan Univ, Key Lab Green Chem & Technol, Coll Chem, Chengdu 610064, Sichuan, Peoples R China; [Tang, Shaojian; Wei, Wenjing; Yin, Dan; Poznik, Michal; Chruma, Jason J.] Sichuan Univ, Sino British Mat Res Inst, Coll Phys Sci & Technol, Chengdu 610064, Sichuan, Peoples R China in 2019.0, Cited 43.0. Name: 3-Pyridinecarboxaldehyde. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1
A palladium-catalyzed decarboxylative propargylation (DcPg) of propargyl 2,2-diphenylglycinate imines was developed. In this process, the nature of the propargyl ester and aryl imine components, as well as the catalyst system and solvent, had a significant impact on the ratio of desired propargylated products vs. allene and/or diene side products that arise via different modes of C-C bond formation. The resulting propargylated products can be transformed readily into useful (Z)-homoallylic amines. Moreover, the regioisomeric diene products could be converted to pharmaceutically-relevant diarylmethyl imines via a two-step Diels-Alder/oxidation process.
Name: 3-Pyridinecarboxaldehyde. Welcome to talk about 500-22-1, If you have any questions, you can contact Tang, SJ; Wei, WJ; Yin, D; Poznik, MC; Chruma, AO or send Email.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem