| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220786 | Tetrahedron | 2011 | 6 Pages |
Abstract
2-Aryl-1,9-dihydrochromeno[3,2-d]imidazoles were prepared by a one-pot cascade reaction involving salicylaldehydes and arylideneaminoacetonitriles. These novel compounds were isolated in 11–95% yield after reflux in ethanol and triethylamine. A dimeric structure was also identified and partially evolved to the tricyclic product in DMSO solution, according to an evolution study by 1H NMR spectroscopy.
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