A Convenient Synthesis of 4-(2-Furyl)-2-substituted Thiazoles Utilising [Hydroxy(tosyloxy)iodo]benzene

A facile synthesis of 4-(2-furyl)-2-substituted thiazoles by hypervalent iodine oxidation of 2-acetylfuran (1) using [hydroxy(tosy-loxy)iodo]benzene, followed by treatment of the reaction mixture with appropriate thioureas/thioamides is described.     

FTIR and circular dichroism spectroscopic study of interaction of 5-fluorouracil with DNA

5-Fluorouracil (5FU) is an anticancer chemotherapeutic drug which exerts cytotoxic effect by inhibiting cellular DNA replication. In the present study, we explore the binding of 5FU with DNA and resulting structural and conformational changes on DNA duplex. UV-visible, Fourier transform infrared (FTIR) and circular dichroism (CD) spectroscopic techniques were employed to explore these interactions. A constant concentration of calf thymus DNA was incubated with varying concentrations of 5FU. UV-visible and FTIR spectroscopic results revealed that intercalation is the primary mode of interaction between 5FU and nitrogenous bases of the nucleic acid. The binding constant was found to be 9.7×10(4); which is indicative of moderate type of interaction between 5FU and DNA duplex. It was also observed that 5FU intercalates slightly more between AT base pairs compared to GC pairs. FTIR and circular dichroism spectroscopic results revealed that 5FU disturbs native B-conformation of DNA though, DNA remains in its B conformation even at higher concentrations of 5FU.     

Observation of Gouy phase anomaly with an interferometer

The intensity variation of bright and dark fringes in Young's double slit experiment shows that a light beam propagating through the focus of a lens experiences a phase shift (called the Gouy phase shift [Gouy CR. Acad Sci Paris 1890;110:1251]) with respect to its plane wave counterpart. The additional phase change of π introduced on focusing the light beam and then further propagating it in one arm of the interferometer changes a bright fringe into a dark fringe and vice-versa. We have, thus, made direct visualization of the Gouy phase shift by a simple experiment.     

Gas‐Phase Synthesis of 1‐Silacyclopenta‐2,4‐diene

Silole (1‐silacyclopenta‐2,4‐diene) was synthesized for the first time by the bimolecular reaction of the simplest silicon‐bearing radical, silylidyne (SiH), with 1,3‐butadiene (C₄H₆) in the gas phase under single‐collision conditions. The absence of consecutive collisions of the primary reaction product prevents successive reactions of the silole by Diels–Alder dimerization, thus enabling the clean gas‐phase synthesis of this hitherto elusive cyclic species from acyclic precursors in a single‐collision event. Our method opens up a versatile and unconventional path to access a previously rather obscure class of organosilicon molecules (substituted siloles), which have been difficult to access through classical synthetic methods.     

Controlled Quantum Teleportation of Superposed Coherent State Using GHZ Entangled Coherent State

Controlled quantum teleportation of superposed coherent states using GHZ entangled 3-mode coherent states is studied. Proposed scheme can be implemented experimentally using linear optical components such as a symmetric lossless beam splitter, two phase-shifters and two photon counters. Fidelity is found close to unity for appreciable mean number of photons in coherent states and is 0.99 for mean photon number equal to two.

     

The Thioesterase of the Erythromycin-Producing Polyketide Synthase: Influence of Acyl Chain Structure on the Mode of Release of Substrate Analogues from the Acyl Enzyme Intermediates

The production of genetically engineered polyketides depends critically on thioesterase activity for product release. In vitro studies with the thioesterase from the erythromycin polyketide synthase (PKS) have demonstrated that the ability of this enzyme to act as a universal decoupler is limited, but stereochemical variation is readily tolerated. Synthetic analogues with all four stereochemical configurations of the natural substrate's 2-methyl-3-hydroxy substitution pattern ( 1 – 4 ; X=p-nitrophenoxy) were substrates for the enzyme.     

The Influence of Film Coating on the Surface Roughness and Specific Surface Area of Pellets

The aim of this paper was to study the surface roughness of pellets after the application of a film coat. In total eight batches of pellets were examined of which four were considered to be round, whereas the other four deviated from the spherical shape by various degrees. The determination of the specific surface area of the coated pellets suggested that, although the film appeared to have filled the pores, the final film structure still mirrored the original surface structure of the pellets. However, profilometry was able to evaluate these gross results in more detail. From the latter measurements it appeared as though the pellet shape was another major influence factor on the final surface texture of the film coating. Pellets with a more elongated and irregular shape such as dumbbells provided more possibilities for interparticulate contact during the coating process, whereby film forming material was ripped off the pellet surfaces making these appear more rough due to surface defects. The use of alcoholic binder solutions during the pellet production might have resulted in surfaces with slightly changed surface free energy, which allowed a better spreading and adhesion of the polymer film and resulted in less textured film surfaces.     

Studies on the process variables of the condensation reaction of cardanol and formaldehyde by response surface methodology

Different types of cardanol-based novolac-type phenolic resins are produced under a wide range of operating conditions for the application in the resin producing industries. Different operating conditions employed for the production of such resins result in different extent of conversion. In order to understand the system behavior, mathematical relationship between the process variables and the extent of conversion was established by employing the ‘Response surface methodology’. Geometrical representation of the mathematical models in three-dimensional surface plots served as a good aid in understanding the behaviour of reaction under different operating conditions. The maximum extent of conversion of the condensation reaction of cardanol and formaldehyde was found to be 93.0 percent at optimum sets of condition of reaction temperature, time, catalyst concentration and pH of the reaction mixture. All the predicted values for optimum process conditions were in good agreement with experimental data.