Pyridone Directed Ru-Catalyzed Olefination of <i>sp</i><sup>2</sup>(C–H) Bond Using Michael Acceptors: Creation of Drug Analogues
Smruti Ranjan Mohanty, Namrata Prusty, Tanmayee Nanda, Shyam Kumar Banjare, Ponneri C. Ravikumar
Abstract
-arylpyridones has been demonstrated, where the pyridone was utilized as a weakly coordinating directing group. Importantly, the current methodology has been effectively applied to the synthesis of many drug analogues such as pirfenidone, naproxen, ibuprofen, geraniol, umbelliferone, pregnenolone, and estrone. This methodology tolerates a wide range of functional groups and yields up to 93% yield. A six-membered ruthenium complex was also detected by HRMS.
Topics & Concepts
ChemistryRutheniumRegioselectivityCatalysisYield (engineering)NitrileMedicinal chemistryMichael reactionStereochemistryAlkylationCombinatorial chemistryOrganic chemistryMaterials scienceMetallurgyCatalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsSulfur-Based Synthesis Techniques