91091-21-3Relevant articles and documents
A convenient synthesis of 4-aminoaryl substituted cyclic imides
Mederski, Werner W.K.R.,Baumgarth, Manfred,Germann, Martina,Kux, Dieter,Weitzel, Thomas
, p. 2133 - 2136 (2003)
An efficient one-step synthesis of 4-nitro-N-aryl substituted glutarimides, succinimides and maleimides in polyphosphoric acid is described together with the subsequent reduction to the corresponding anilines. The scope and limitation of this cyclocondensation are presented.
A convenient one-pot synthesis of polysubstituted pyrroles from N-protected succinimides
Kobeissi, Marwan,Yazbeck, Ogaritte,Chreim, Yamama
supporting information, p. 2523 - 2526 (2014/05/06)
The dienamine products formed by the reaction between polysubstituted succinimides and the Petasis reagent were subjected to isomerization under mild acidic conditions to give polysubstituted pyrroles in excellent yields (85-95%). The scope and limitations of this methodology are explored.