38614-32-3Relevant academic research and scientific papers
Synthesis, X-ray crystallography, and reactions of N-acyl and N-carbamoyl succinimides
Goodman, Cassie A.,Eagles, Joel B.,Rudahindwa, Leandre,Hamaker, Christopher G.,Hitchcock, Shawn R.
supporting information, p. 2155 - 2164 (2013/07/25)
A collection of N-acyl and N-carbamoyl succinimides were prepared by acylation of succinimide with acyl chlorides or by ethylene dichloride (EDC) coupling of carboxylic acids. The x-ray crystal structures of N-benzoyl and N-p-nitrobenzoyl succinimides were determined. The N-acyl succinimides were effective in acylating primary amines, a secondary amine, and an aromatic amine. Copyright
Some unusual reactivities in the SmI2-mediated reductive coupling of acrylamides and acrylates with imides
Taaning, Rolf H.,Lindsay, Karl B.,Skrydstrup, Troels
experimental part, p. 10908 - 10916 (2010/02/27)
A serendipitous discovery of some intra-molecular enolate addition reactions following a SmI2-mediated reductive cross-coupling between imides and electron-deficient olefins leading to some novel compounds was investigated to determine the generality of the protocol and the possible mechanistic pathways involved. This provided a Z-selective synthesis of γ-ketoenediamides in good yields, albeit as of now the substrate scope remains limited. It was also shown that the seemingly similar acrylate substrates can behave differently compared to the corresponding acrylamides in their SmI2-mediated reductive cross-coupling reaction with imides, and it was argued that these diverging reactivities are dominated by the ability of the acrylates to coordinate the samarium metal centre.
