Esra Findik

Isoeugenol-based novel potent antioxidants: synthesis and reactivity.

We are attempting to develop the novel phenolic synthetic antioxidants aimed at retarding the effects of free radicals and oxidants. The phenolic compounds (7-12) were synthesized by Friedel-Crafts alkylation of isoeugenol (1) and phenol derivatives (2-6) and their structures were determined by spectroscopic methods. All the synthesized phenolic compounds (7-12) except 12 are new. Antioxidant and radical scavenging activities of synthesized compounds (7-12) were determined by using various in vitro assays such as 1,1-diphenyl-2-picrylhydrazyl free radicals (DPPH), 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) radicals (ABTS(+)), and superoxide anion radicals (O(2)(-)) scavenging, ferric reducing antioxidant power (FRAP) and total antioxidant activity by ferric thiocyanate. The antioxidant activities of compounds were compared with standard antioxidants such as butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT) and trolox as positive controls. The results showed that the synthesized compounds, especially 10 and 11, had better properties than standard antioxidants (BHT, BHA and trolox).

Synthesis of 3‐Aryl‐2‐benzoylbenzofuran Derivatives using Manganese(III) Acetate–Mediated Addition of Dimedon to Chalcone Derivatives

Abstract 3‐Aryl‐2‐benzoylbenzofurans were synthesized by the reaction of α‐carboradical produced from dimedon by oxidizing with manganese(III) acetate in acetic acid and the chalcone derivatives.

Synthesis and Characterization of New Chalcone Derivatives from cis-Bicyclo[3.2.0]hept-2-en-6-one

Abstract A series of chalcone derivatives (3a–k) were prepared via the reaction of cis-bicyclo[3.2.0]hept-2-en-6-one (1) with the respective arylaldehydes (2a–k) and were then characterized by Fourier transform infrared (FT-IR), 1H NMR, 13C NMR, and elemental analyses.

Cyclohexenones Through Regioselective Addition of 1,3-Dicarbonyl Compounds to Terpenoid-Like Bischalcones

Abstract Terpenoid-like bischalcones (3 and 4) were synthesized from the reaction of α- and β-ionones and benzaldehydes in excellent yields. The Michael addition of 1,3-dicarbonyl compounds to bischalcones (3 and 4) resulted in the formation of cyclohexenones derivatives (10a–d and 14a, b) via regioselective addition of 1,3-dicarbonyls and then cyclization.

Synthesis of Terpenoid-Like Bischalcones from α- and β-Ionones and Their Biological Activities

Abstract Ionone-based terpenoid-like bischalcones (3a–h and 4a–h) were synthesized from the reaction of α- and/or β-ionones with aldehyde derivatives in excellent yields. The antibacterial activities of synthesized compounds were screened against human pathogenic micro-organisms by employing the disk-diffusion technique.

Four-Component, One-Pot Synthesis of 2-Aryl-4-Thionylquinoline Derivatives and Their Aromatization

Abstract Four-component, one-pot condensation of dimedon, thiophene-2-carbaldehyde, ammonium acetate, and numerous acetophenones yielded novel 2-aryl-4-thionylquinoline derivatives. The structures were characterized by 1H NMR, 13C NMR, IR, and elemental analysis.