In 2019.0 ORG BIOMOL CHEM published article about MULTICOMPONENT REACTIONS; CONVERTIBLE ISOCYANIDE; RAPID ACCESS; CONDENSATION in [Kurva, Mahanandaiah; Kerim, Mansour Dole; El Kaim, Laurent] Ecole Polytech, Inst Polytech Paris, Lab Synth Organ, CNRS,ENSTA Paris,UMR 7652, 828 Bd Marechaux, F-91128 Palaiseau, France; [Kurva, Mahanandaiah; Gamez-Montano, Rocio] Univ Guanajuato, Dept Quim, Noria Alta S-N, Guanajuato 36050, Gto, Mexico in 2019.0, Cited 36.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. Product Details of 500-22-1
The Ugi reaction of 2-nitrobenzoic acid derivatives has been used for a diversity oriented synthesis of complex isoindolinones via a SNAr reaction involving the peptidyl position. When the cyclization is triggered by strong bases such as potassium tert-butylate, the SNAr reaction is followed by a deamidification/oxidation sequence leading to 2-hydroxyisoindolinones. The latter may be further transformed into polycyclic fused isoindolinones via Pictet-Spengler type cyclization or O-alkylation/metathesis sequences.
Welcome to talk about 500-22-1, If you have any questions, you can contact Kurva, M; Kerim, MD; Gamez-Montano, R; El Kaim, L or send Email.. Product Details of 500-22-1
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem