In 2020.0 CHEM-EUR J published article about N-HETEROCYCLIC CARBENE; STEREOSELECTIVE-SYNTHESIS; CONJUGATE ADDITIONS; ENOLATE ADDITIONS; STETTER REACTION; CATALYSIS; ESTERS; HYDROGENATION; ALDEHYDES; COMBINATION in [Maskeri, Mark A.; Schrader, Malte L.; Scheidt, Karl A.] Northwestern Univ, Dept Chem, Ctr Mol Innovat & Drug Discovery, Silverman Hall, Evanston, IL 60208 USA in 2020.0, Cited 85.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. Formula: C6H5NO
Combining biological and small-molecule catalysts under a chemoenzymatic manifold presents a series of significant advantages to the synthetic community. We report herein the successful development of a two-step/single flask synthesis of gamma-lactones through the merger of Umpolung catalysis with a ketoreductase-catalyzed dynamic kinetic resolution, reduction, and cyclization. This combined approach delivers highly enantio- and diastereoenriched heterocycles and demonstrates the feasibility of integrating NHC catalysis with enzymatic processes.
Welcome to talk about 500-22-1, If you have any questions, you can contact Maskeri, MA; Schrader, ML; Scheidt, KA or send Email.. Formula: C6H5NO
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem