100994-75-0Relevant academic research and scientific papers
Carbonylation of β-Aminoethanols, Diols, and Diol Amines
Tam, Wilson
, p. 2977 - 2981 (1986)
Oxazolidinones are prepared from the palladium-catalyzed carbonylation of β-aminoethanols under mild conditions.With N-alkyl-substituted substrates, conditions for double carbon monoxide incorporation to give morpholinediones have been discovered.Cyclic carbonates can be prepared from the carbonylation of diols.The carbonylation of N-phenyl-1-aminopropane-2,3-diol can give either the carbonate or oxazolidinone as the major product depending on the reaction conditions.
The reaction of glycerol carbonate with primary aromatic amines in the presence of Y- and X-faujasites: The synthesis of N-(2,3-dihydroxy)propyl anilines and the reaction mechanism
Selva, Maurizio,Fabris, Massimo
experimental part, p. 1161 - 1172 (2010/05/18)
At 140 °C, in the presence of alkali metal exchanged faujasites, preferably NaY, as catalysts, glycerine carbonate (GlyC) is an efficient and green alkylating agent of primary aromatic amines (p-XC6H 4NH2, X = H, OMe, OH,
