1111659-29-0Relevant academic research and scientific papers
Synthesis of unsymmetrical (1,3-diarylimidazolidin-4-yl) (aryl)methanone via Mannich reaction
Kaladevi, Selvam,Paul, Nidhin,Muthusubramanian, Shanmugam,Sivakolunthu, Subbiah
supporting information, p. 3702 - 3705 (2013/07/05)
An atom-efficient, catalyst-free and environmentally friendly approach towards the synthesis of 1,3,4-trisubstituted imidazolidines (4a-4p) through a multicomponent reaction involving monophenacyl anilines 1, aromatic amines 2 and formaldehyde 3 has been developed. The reaction proceeds in refluxing ethanol providing higher yields of the imidazolidines.
Rearrangements of tetrahydroimidazo[1,5-b]isoxazole-2,3-dicarboxylates to pyrrolo[1,2-e]imidazol-6-ols, precursors of 2,5-dihydro-1H-pyrrole derivatives
Co?kun, Necdet,?etin, Meliha
experimental part, p. 648 - 658 (2009/04/07)
Isoxazolines 2 from the cycloaddition of imidazoline 3-oxides 1 with DMAD rearrange in the presence of methoxide to give cis-3-methoxy-7-(methoxycarbonyl)-2,7a-diaryl-5-oxo-2,3,5,7a-tetrahydro-1H-pyrrolo[1,2-e]imidazol-6-olates 3 with 100% de. The acidic
