The electrochemical oxidation of iodide ion in the presence of 4-hydroxycoumarin (1) was studied using cyclic voltammetry and controlled-potential coulometry. The result indicates that the resulting iodine takes part in a halogenation reaction and reacts with 4-hydroxycoumarin (1). According to the obtained results, a new and simple coulometric titration method with potentiometric end-point det...

Reactions of 4-hydroxycoumarin 1 with heterocyclic aldehydes 2-4 led to bis-4-hydroxycoumarin derivatives 5-7 under microwave irradiation as well the classical heating. The subsequent reactions products are described. 4,4’-Epoxydicoumarins 8, 9 were prepared by reaction in acetic acid / p-toluenesulfonic medium. Compound 10 was 5 anhydride presence sodium acetate. Dioxocine-1,15-dione 11 6 dich...

Abstract The preparation 0f azo dyes is the subject of this research. 4-hydroxycoumarin with each ofo-amino benzoic acid (3-[o-Amino acidazo]-4-hydroxycoumarin]) (B 1 ) and Sulfa guanidine (3-[Sulfa azo]-4-hydroxycoumarin) 2 were syntheses. Azo compounds characterized by I.R, CHN, H-NMR Elctronic Mass spectroscopy. At various pH levels, electronic spectra these investigated in terms acid-base p...

Some novel coumarins were synthesized starting from 4-hydroxycoumarin and methyl bromoacetate. The structures of the newly obtained compounds were confirmed by elemental analysis, mass, IR and NMR spectra.

Warfarin is often used as a site-specific probe for examining the binding of drugs and other solutes to Sudlow site I of human serum albumin (HSA). However, warfarin has strong binding to HSA and the two chiral forms of warfarin have slightly different binding affinities for this protein. Warfarin also undergoes a slow change in structure when present in common buffers used for binding studies....

A concise and efficient one-pot synthesis of 3-functionalized 4-hydroxycoumarin derivatives via a three-component domino reaction of 4-hydroxycoumarin, phenylglyoxal and 3-arylaminocyclopent-2-enone or 4-arylaminofuran-2(5H)-one under catalyst-free and microwave irradiation conditions is described. This synthesis involves a group-assisted purification process, which avoids traditional recrystal...

Micro-organisms have been isolated that can utilize o-coumaric acid as a sole carbon source with the subsequent production of 4-hydroxycoumarin and dicoumarol. One of these organisms, Penicillium jenseni, has been used to examine the biosynthesis of dicoumarol. Certain thermophilic fungi have also been found that can convert o-coumaric acid into dicoumarol.