Evaluation of In Silico and In Vitro Antidiabetic Properties of 4-(Hydroxysubstituted Arylidene)-2-Phenyloxazol-5(4<i>H</i>)-one Derivatives. [PDF]
Jayasinghe RN +5 more
europepmc +1 more source
Prebiotic chiral transfer from self-aminoacylating ribozymes may favor either handedness. [PDF]
Kenchel J +10 more
europepmc +1 more source
Oxazole and isoxazole-containing pharmaceuticals: targets, pharmacological activities, and their SAR studies. [PDF]
Li S +5 more
europepmc +1 more source
Non-enzymatic reactions in biogenesis of fungal natural products. [PDF]
Kishimoto S.
europepmc +1 more source
Stereoselective Synthesis of Axially Chiral Allenes and Styrenes via Chiral Phosphoric Acid Catalysis: An Overview. [PDF]
Woldegiorgis AG +5 more
europepmc +1 more source
Exploring of novel oxazolones and imidazolones as anti-inflammatory and analgesic candidates with cyclooxygenase inhibitory action. [PDF]
Rayan SA +3 more
europepmc +1 more source
NHC-catalyzed asymmetric synthesis of natural products and pharmaceutical drugs. [PDF]
Shahid A +9 more
europepmc +1 more source
5‐Oxazolones, IV. Reactions of 5(4H)‐oxazolones with triphenylphosphonium methylides
AbstractThe Wittig reaction of ethyl (triphenylphosphoranylidene)acetate (2a) with the carbonyl group of trisubstituted 5(4H)‐oxazolones 1a–c afforded ethyl 5(4H)‐oxazolylideneacetates 3a–c and triphenylphosphane oxide. Starting from oxazolones 1d–i and ylide 2a, methyleneoxazoles 3d, e and ethyl 5‐oxazoleacetates 4a–f were obtained besides ylides 5a–e
E. Erba, M.L. Gelmi, D. Pocar
openaire +3 more sources
On the Reactivity of 5(4H)-Oxazolones with Amines
Peer ...
Blasco, Javier +5 more
openaire +3 more sources
Synthesis and Characterization of Carbazolyl-Oxazolones
In this study, the synthesis of 2-carbazolyl-4-aryl/heteroarylidene-5-oxazolones (3a-k) derivatives starting from carbazole glycine ester I derivatives (1a-b) was described. Thus, we aimed to combine the advantages of carbazole and 5-oxazolone moieties in synthesis of 2-carbazolyl-4-aryl/heteroarylidene-5-oxazolones (3a-k). These derivatives (3a-k) may
Gocmenturk, Mustafa +2 more
core +3 more sources

