1049784-75-9Relevant academic research and scientific papers
Selective reduction of carbonyl amides: Toward the first unsymmetrical bischelating N-substituted 1,2-diamino-4,5-diamidobenzene
Seillan, Claire,Braunstein, Pierre,Siri, Olivier
experimental part, p. 3113 - 3117 (2009/04/10)
Selective reduction of carbonyl amides from key tetraamido intermediate 12 afforded an unprecedented N-substituted 1,2-diamino-4,5-diamidobenzene (13) and/or the first member (14) of a new family of unsymmetrical 12π-electron quinonediimines. Wiley-VCH Ve
