Experiments were conducted to characterize the metabolism of ezlopitant alkene (CJ-12,458), an active metabolite of ezlopitant, in human liver microsomes. In incubations with human liver microsomes and cofactors required for cytochrome P450 (CYP) activity, CJ-12,458 was converted to two metabolites: a diol (CP-611,781) and a 1 degrees alcohol (CP-616,762). In human liver microsomes, apparent K(...

The main focus of the current research is bio-nano-technologically produced nanoparticles (NPs) utilizing waste materials. There a need for developing advanced technology to reduce in an eco-friendly way. Therefore, presently discarded aqueous portion Prosopis cineraria pod was used after boiling, synthesize Ag and Ag–Cu NPs. FT-IR spectra illustrated presence phenyl propenoids flavonoids displ...

A new class of sterically hindered dendrimer-metalloporphyrins was synthesized for use as shape-selective oxidation catalysts. A series of oxidatively robust poly(phenylesters) dendrimers were prepared through a convergent synthesis. Monodendrons were appended to the meta-positions of the 5,10,15,20-tetrakis(3′,5′-hydroxyphenyl)porphinatomanganese(III) chloride to obtain a sterically protected ...

The mechanism of alkene epoxidation by chromium(v) oxo salen complexes has been studied by DFT and experimental methods. The reaction is compared to the closely related Mn-catalyzed process in an attempt to understand the dramatic difference in selectivity between the two systems. Overall, the studies show that the reactions have many similarities, but also a few critical differences. In agreem...

Chiral MnIII (salen) complex supported on modified ZPS-PVPA (zirconium poly(styrenephenylvinylphosphonate)) and ZPS-IPPA (zirconium poly(styrene-isopropenyl phosphonate)) were prepared using –CH2Cl as a reactive surface modifier by a covalent grafting method. The supported catalysts showed higher chiral induction (ee: 72%–83%) compared with the corresponding homogeneous catalyst (ee: 54%) for a...

imidazole, which functions as an axial ligand for Mn'". This system was used to catalyze the epoxidation of water-soluble (2,5-dihydrofuran, 3) and -insoluble (styrene, 4) alkene^.^ The reactions followed first-order kinetics. GCMS and comparison with authentic samples showed that for 3 the reaction products are 3,4-epoxytetrahydrofuran and the ring-opened compound trans-3,4-dihydroxytetrahydro...

Aerobic partial oxidations of alkanes and alkenes are important processes of the petrochemical industry. The radical mechanisms involved can be catalyzed by soluble salts of transition metals (Co, Cu, Mn...). We show here that the model methylcyclohexane/stilbene co-oxidation reaction can be efficiently catalyzed at lower temperature by supported gold nanoparticles. The support has little influ...

Alkene monooxygenase (AMO) from Rhodococcus rhodochrous B-276 is a 3-component enzyme system encoded by the 4-gene operon amoABCD, which catalyzes the stereoselective epoxidation of aliphatic alkenes yielding primarily the R enantiomer. With propene as the substrate, wild-type AMO yields R-epoxypropane with an enantiomeric excess (e.e.) of 83%. The presumed site of alkene oxidation is a dinucle...

An overview of the synthesis and applications of chiral 2,3-epoxy alcohols containing unsaturated chains is presented. One of the fundamental synthetic routes to these compounds is Sharpless asymmetric epoxidation, which is reliable, highly chemoselective and enables easy prediction of the product enantioselectivity. Thus, unsaturated epoxy alcohols are readily obtained by selective oxidation o...