Sodium borohydride reduction of aromatic carboxylic acids via methyl esters

A number of important aromatic carboxylic acids precursors, or intermediates in the syntheses of natural products, are converted into methyl esters and reduced to the corresponding primary alcohols using a sodium borohydride-THF-methanol system. The alcohols are obtained in 70–92% yields in 2–5 hours, in a pure state. This two-step procedure not only provides a better alternative to aluminum hydride reduction of acids but also allows the selective reduction of esters in presence of acids, amides, nitriles or nitro functions which are not affected under these conditions.     

Substituent effects on novel diaminovinylidenes by DFT

Research on Chemical Intermediates - Electronic and steric effects on singlet and triplet symmetric 2,4-diX-vinylidenes with acyclic, cyclic-saturated, and cyclic-unsaturated structures are...     

Synthesis of novel 5,6,7,8,9,10-hexahydropyrimido[4,5-b]quinoline derivatives for antimicrobial and anti-oxidant evaluation

Because of the well-known chemotherapeutic activity of pyrimidoquinolines, a new series of the title compounds were synthesized and biologically screened for their antimicrobial and anti-oxidant activities. The intermediate compound, 2-amino-1-cyclohexyl-4-(3,4-dimethoxyphenyl)-1,4,5,6,7,8-hexahydroquinoline-3-carbonitrile (2), was prepared and allowed to react with oxalyl chloride to give the corresponding strategic starting material, 10-cyclohexyl-5-(3,4-dimethoxyphenyl)-4-oxo-3,4,5,6,7,8,9,10-octahydropyrimido[4,5-b]quinoline-2-carbonyl chloride 3. Compound 3 underwent diverse reactions with amines to give the corresponding carboxylic amides 4, with alcohols to give the carboxylic esters 5 and with hydrazine to give the carbohydrazide 8. Compound 8 reacted with aldoses to give the corresponding polyhydroxy(-)alkyl Schiff bases 9, which upon reaction with thioglycolic acid afforded the thiazolidinone-C-acyclic nucleosides 10. Several other pyrimidoquinolines incorporated to oxadiazole, iminothiazolidinones and thiadiazoles were synthesized starting from the 2-carbohydrazide derivative 8. Most of the newly prepared derivatives showed considerable antimicrobial activity against Gram +ve and Gram ?ve bacteria and anti-oxidant activity.     

Velocity measurements in jets with application to noise source modeling

This paper describes an experimental investigation of the statistical properties of turbulent velocity fluctuations in an axisymmetric jet. The focus is on those properties that are relevant to the prediction of noise. Measurements are performed using two single hot-wire anemometers as well as a two-component anemometer. Two-point cross correlations of the axial velocity fluctuations and of the fluctuations in the square of the axial velocity fluctuations are presented. Several reference locations in the jet are used including points on the jet lip and centerline. The scales of the turbulence and the convection velocity are determined, both in an overall sense as well as a function of frequency. The relationship between the second and fourth order correlations is developed and compared with the experimental data. The implications of the use of dimensional as well as non-dimensional correlations are considered. Finally, a comparison is made between the length scales deduced from the flow measurements and a RANS CFD calculation.     

Effects of Hall current on unsteady MHD flows of a second grade fluid

The aim of this present paper is to construct exact solutions corresponding to the motion of magnetohydrodynamic (MHD) fluid in the presence of Hall current, due to cosine and sine oscillations of a rigid plate as well as those induced by an oscillating pressure gradient. A uniform magnetic field is applied transversely to the flow. By using Fourier sine transform steady state and transient solutions are presented. These solutions satisfy the governing equations and all associated initial and boundary conditions. The results for a hydrodynamic second grade fluid can be obtained as a limiting case when B ₀ → 0 and for a Newtonian fluid when α ₁ → 0.