4345-33-9Relevant academic research and scientific papers
Synthesis of Fused Oxazolocoumarins from o-Hydroxynitrocoumarins and Benzyl Alcohol Under Gold Nanoparticles or FeCl3 Catalysis
Vlachou, Evangelia-Eirini N.,Armatas, Gerasimos S.,Litinas, Konstantinos E.
, p. 2447 - 2453 (2017)
Synthesis of fused oxazolocoumarins has been achieved from the one-pot tandem reactions of o-hydroxynitrocoumarins with benzyl alcohol in toluene under catalysis in a sealed tube at 150°C. The catalysis was performed by gold nanoparticles supported on TiO
Tricyclic heteroaromatic systems. Synthesis and benzodiazepine receptor affinity of 2-substituted-1-benzopyrano [3,4-d] oxazol-4-ones, -thiazol-4- ones, and -imidazol-4-ones
Colotta, Vittoria,Catarzi, Daniela,Varano, Flavia,Cecchi, Lucia,Filacchioni, Guido,Martini, Claudia,Giusti, Laura,Lucacchini, Antonio
, p. 375 - 381 (2007/10/03)
A number of 2-aryl-substituted-1-benzopyrano [3,4-d] oxazol-4-ones 1, - thiazol-4-ones 2 and -imidazol-4-ones 3 were synthesized. Benzodiazepine receptor (BZR) binding assays were performed on these series of tricyclic heteroaromatic systems. None of the tested compounds showed detectable affinity for BZR. Comparative structure-activity relationship analysis between the reported compounds and some known BZR ligands of similar size and shape revealed that, according to a two-dimensional schematic representation of the interaction of these kinds of tricyclic heteroaromatic systems with the BZR recognition site, the nature of the optional a~ proton acceptor is of significant importance in the receptor-ligand interaction.
