Aqueous phase fly-ash catalyzed [4+2] Diels-Alder reaction of aryl enones and cyclopentadiene: Synthesis and insect antifeedant activities of aryl bicyclo [2.2.1] heptene-2-yl-methanones

A series containing ten aryl 3-(substituted phenyl) bicyclo [2.2.1] heptene-2-yl-methanone derivatives including 3- (substituted phenyl) bicyclo [2.2.1]hepten-2-yl-(pyren-1-yl)- methanones have been synthesized by aqueous phase fly-ash catalyzed [4+2] Diels-Alder cyclo addition reaction of cyclopentadiene and aryl chalcones. The yields of the methanones are more than 60%. The synthesized methanones are characterized by their physical constants and spectral data. The insect antifeedant activities of synthesized methanones have been studied using Dethler’s leaf-discs bioassay method

Hydroxyapatite Catalyzed Cyclization of Aryl Enones: Solvent-Free Efficient Synthesis of Some 4-Aryl-5,6-Dihydro-6-(Substituted Phenyl)-4H-1,3-Oxazine-2-Amines

Some 4-aryl-5,6-dihydro-6-(substituted phenyl)-4H-1,3-oxazine- 2-amine derivatives including 4-(4-methyl-1-naphthyl)-5,6- dihydro-6-(substituted phenyl)-4H-1,3-oxazine-2-amines have been synthesised by hydroxyapatite catalyzed solvent-free cyclization of aryl chalcones and urea using microwave irradiation under solventfree condition. The yields of the oxazines were more than 85%. The synthesised oxazine amines have been characterized by their physical constants, analytical and spectroscopic data

Synthesis, spectral studies and insect antifeedant activities of some 4-substituted 1-naphthacyl bromide and its esters

About nine 4-substituted 1-naphthacyl bromides and its esters have been synthesized by greener synthetic method using fly-ash catalyzed water mediated reaction.  These acyl bromides and esters have been characterized by their physical constants, Mass, IR and NMR spectral data.  These carbonyl frequencies(cm-1) of existed rotomers of these compounds have been assigned and correlated with Hammett substituent constants, F, R and Swain-Lupton’s parameters.  The insect antifeedant activities of the synthesized acyl bromide and esters have been evaluated using 4th instar larvae Achoea Janatha L

Synthesis of Schiff’s bases of 2-amino benzo[d]thiazole from higher hetero aldehydes and ketones using Mo-Al2O3 composite based organo catalyst

We have used a new metal supported organo catalyst successfully to carry out the high yield Schiff’s base reaction at ambient temperature. This methodology has the benefits of straightforward conditions, excellent yields, no work-up, environmental benign process and reusable solid catalyst. The catalyst speeds up the Schiff base reaction with less time and several Schiff bases were synthesised and given IR,1H,13C NMR characterisation

A facile designed highly moderate craspedia flowerlike sulphated Bi2O3-fly ash catalyst: Green synthetic strategy for (6H-pyrido[3,2-b]carbazol-4-yl)aniline derivatives in water

AbstractThe air pollutant fly ash was facile designed as a green catalyst and practical to organic synthesis. We have designed sulfated Bi2O3-fly ash catalyst (12wt%) and it was characterized by Fourier transform infrared (FT-IR), confocal Raman, Powder X-ray diffraction (XRD), Field emission electron microscopy (FE-SEM), elemental color mapping, energy-dispersive X-ray spectroscopy (EDS), Transmission electron microscopy (TEM) and Brunauer–Emmett–Teller (BET) techniques. The sulfated Bi2O3-fly ash was found an excellent catalytic application for the synthesis of (6H-pyrido[3,2-b]carbazol-4-yl)aniline derivatives in water has been described. The synthesized (6H-pyrido[3,2-b]carbazol-4-yl)aniline derivatives were confirmed by spectral techniques Fourier transform infrared (FT-IR), Nuclear magnetic resonance (NMR) and Liquid chromatography–mass spectrometry (LC–MS). The significant catalytic role of Bi–N interaction was readily form adduct, moreover Bi–O bond was favorable for hydrogen abstraction, dehydration and aromatization. Due to the strong potential, the precise reaction time and high yield have been achieved, which is realized from hot filtration test. The sulfated Bi2O3-fly ash catalyst could be reused for five successive run, the resulting in no appreciable change in the catalytic activity. The crystal phase and surface morphology of fifth run catalyst were examined by powder XRD, FE-SEM, EDS and TEM techniques, and the results revealed no changes in catalyst nature. The sulfated Bi2O3-fly ash catalyst has high efficiency, reusability, good catalytic activity, environmentally harmless and notable potential in industrial applications

Spectral LFER studies in some N-(substituted phenyl) formamides

A series of N-(substituted phenyl) formamides were synthesised by sulphated titania (TiO2-SO4 2-) catalyzed formylation of substituted anilines and formic acid in acetonitrile medium at room temperature. The synthesised formamide derivatives are characterized by their spectral data. The infrared νNH, CO (cm-1) stretches, chemical shifts(δ, ppm) of NH, COH and ipso carbons(Ar-C-NH) were assigned and correlated with Hammett substituent constants using single and multi-regression analysis. From the results of statistical analyses, the effect of substituents on the spectral data have been studied

Synthesis, assessment of substituent effect and antimicrobial activities of some substituted (E)-Nbenzylidene- 5-bromopyridin-2-amines

A series of substituted (E)-N-benzylidene-5-bromopyridin-2-amine compounds have been synthesized from 5-bromo-2-aminopyridine with different substituted benzaldehydes. The structure of the adducts was confirmed by their physical constants, UV, IR and NMR spectral data. The observed UV absorption maximum λmaxC=N(nm), IR frequencies νC=N(cm-1), The 1H and 13C NMR δ(ppm) chemical shifts values have been correlated with Hammett substituent constants and F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the spectral data has been studied. The antimicrobial activities of all synthesized imines have been studied using Bauer-Kirby method

Solid acidic FeCl3/Bentonite catalyzed solvent-free condensation: Synthesis, spectral studies and antimicrobial activities of some aryl hydrazine Schiff’s bases

Some aryl hydrazide derivatives have been synthesized including 1-(3-chloro-4-nitrophenyl)-2-(3-substituted benzylidene) hydrazines by  FeCl3/Bentonite catalyzed solvent-free  condensation of  substituted phenyl hydrazine and aldehydes under microwave irradiation.  The yields of the hydrazides are more than 70%.  The synthesized hydrazides are characterized by the physical constants, micro analysis and spectroscopic data.  Effect of catalyst,  solvent effect  substituent effect and optimization of the catalyst was studied by the percentage of isolated yields.  From the catalyst optimization, the present study catalyst gave the better yield of products.  The antimicrobial activities of all synthesized of 1-(3-chloro-4-nitrophenyl)-2-(3-substituted benzylidene) hydrazines have been evaluated using Bauer-Kirby disc diffusion method

Perchloric Acid Catalyzed Condensation of Amine and Aldehydes: Synthesis and Antibacterial Activities of Some Aryl (E)-Imines

A series of Schiff’s bases (aryl E-imines) have been derived from the perchloric acid catalyzed condensation of aryl amines and substituted benzaldehydes. The yield of the Schiff’s bases are more than 80%. The synthesized Schiff’s bases are characterized by their physical constants, analytical and spectroscopical data. The antibacterial activities of these Schiff’s bases have been studied using Bauer-Kirby method

Synthesis, spectral correlation analysis and evaluation of biological activities of some substituted hydrazones

Some novel substituted hydrazone derivatives of amino guanidine have been synthesized with different substituted benzaldehydes by condensation method. The synthesized hydrazones were characterized by their physical constants, UV, IR and NMR spectra. The spectral data have been correlated with Hammett substituent constants and Swain–Lupton parameters. From the result of statistical analysis, the effects of substituents on the spectral data have been predicted. The antimicrobial activities of these synthesized hydrazone compounds have been screened by Bauer-Kirby method using human pathogenic bacteria and fungal species. The antimicrobial activities of all synthesized hydrazone compounds have shown significant activity