Wu, Xin-Xing published the artcileSelective synthesis of acylated caprolactam via sequential Michael addition/palladium-catalyzed alpha-arylation of ketones, Application In Synthesis of 1468-83-3, the main research area is acylated caprolactam preparation diastereoselective; methyl ketone acrylamide Michael addition alpha arylation palladium catalyst.
A formal [6 + 1] annulation reaction through sequential Michael addition/palladium-catalyzed alpha-arylation of ketones has been developed. This approach provides an efficient route enabling rapid access to diverse acylated caprolactams by the double C-C bond formation of the same site from Me ketones. In addition, the reaction features a broad substrate scope, good functional group tolerance, easy scale-up of reaction and useful transformations of the products.
Organic Chemistry Frontiers published new progress about Acrylamides Role: RCT (Reactant), RACT (Reactant or Reagent). 1468-83-3 belongs to class benzothiophene, name is 3-Acetylthiophene, and the molecular formula is C6H6OS, Application In Synthesis of 1468-83-3.
Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem