Manley, Peter J. published the artcileA new synthesis of naphthyridinones and quinolinones: palladium-catalyzed amidation of o-carbonyl-substituted aryl halides, Computed Properties of 16332-06-2, the main research area is haloaryl aldehyde amide amidation aldol condensation palladium catalyst; naphthyridinone preparation; quinolinone preparation; palladium amidation aldol condensation catalyst.
An alternative to the Friedlaender condensation for the synthesis of naphthyridinones, e.g., I, and quinolinones has been discovered. Palladium-catalyzed amidation of halo aromatics substituted in the ortho position by a carbonyl functional group or its equivalent with primary or secondary amides leads to the formation of substituted naphthyridinones and quinolinones.
Organic Letters published new progress about Aldol condensation. 16332-06-2 belongs to class ethers-buliding-blocks, name is 2-Methoxyacetamide, and the molecular formula is C3H7NO2, Computed Properties of 16332-06-2.
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem