77026-95-0Relevant academic research and scientific papers
N-Amino-exo-3,6-epoxy-1,2,3,6-tetrahydrophthalimide as an active aminoaziridinating agent
Zibinsky, Mikhail,Stewart, Timothy,Prakash, G.K. Surya,Kuznetsov, Mikhail A.
, p. 3635 - 3642 (2009)
N-Amino-exo-3,6-epoxy-1,2,3,6-tetrahydrophthalimide is active in the oxidative aminoaziridination reaction toward alkenes substituted with aryl-, alkyl, and electron-withdrawing groups, providing access to stable derivatives of N-aminoaz-iridine. Yields varied from 19 to 76%, and trans-substituted alkenes reacted faster and gave better yields than cis-alkenes. No products of self-aziridination were isolated.
Hydroarylation reactions of N-acylaminosubstituted tricyclic imides
Gul, Melek,Kulu, Irem,Ocal, Nuket
, p. 345 - 350 (2013/07/26)
The palladium-catalysed hydroarylation of unsaturated N-acylamino- substituted tricyclic imides provided a new stereoselective synthesis of exo-aryl(heteroaryl)-substituted tricyclic N-acylamino imides.
