Search results for "yield"

Studies on the synthesis of heterocyclic compounds. Part IV. Further investigation of the pschorr reaction with some pyrazole derivatives

1980

Thermal decomposition of the diazonium sulfate derived from N-methyl-(1-phenyl-3-methylpyrazol-5-yl)-2-aminobenzamide afforded products formulated as 1-phenyl-3-methyl[2]benzopyrano[4,3-c]pyrazol-5-one (yield 10%), 1,4-dimethyl-3-phenylpyrazolo[3,4-c]isoquinolin-5-one (yield 10%), N-methyl-(1-phenyl-3-methylpyrazol-5-yl)-2-hydroxybenzamide (yield 8%) and 4′-hydroxy-2,3′-dimethyl-1′-phenylspiro[isoindoline-1,5′-[2]-pyrazolin]-3-one (yield 20%). Decomposition of the diazonium sulfate derived from N-methyl-(1,3-diphenylpyrazol-5-yl)-2-aminobenzamide gave products formulated as 7,9-dimethyldibenzo[e,g]pyrazolo[1,5-a][1,3]-diazocin-10-(9H)one (yield 8%), 4-methyl-1,3-diphenylpyrazolo[3,4-c]isoqu…

ChemInform Abstract: High-Yield Formation of Arbutin from Hydroquinone by Cell-Suspension Cultures of Rauwolfia serpentina.

2010

Fast Solution Precursor Synthesis of the 2223 Phase: the Role of Lead in the Reaction Pathway

1994

ABSTRACTValuable mechanistic information, about the reaction pathway in the formation of the 2223 phase, has been obtained by the use of a solution synthesis route. The presence of lead in the starting mixture has remarkable effects on the nature and stability of the different intermediates: i) the grain size and morphology of Bi2CuO4 is severely changed, ii) calcium carbonate is partially decomposed to yield the calcium plumbate, iii) the 2201 phase results stabilized against the formation of the collapsed phase Bi17Sr16Cu7O49-δ, iv) the melting point of the intermediate 2212 is lowered by about 10 °C. All these effects, due to lead substitution, contribute to promote the formation of the …

Steady-state fluorescence emission studies on polyazacyclophane macrocyclic receptors and on their adducts with hexacyanocobaltate(III)

1995

The steady-state fluorescence emission spectra of the azacyclophanes 2,5,8,11-tetraaza[12] paracyclophane (L1), 2,6,9,13-tetraaza[14]paracyclophane (L2), 14,15,17,18-tetramethyl-2,5,8,11-tetraaza[12]paracyclophane (L3) and 16,17,19,20-tetramethyl-2,6,9,13-tetraaza[14]paracyclophane (L4) as a function of pH have been measured. The fully protonated species of each cyclophane gives the highest fluorescence-emission quantum yield. The shapes of the titration curves have been explained by the existence of an electron-transfer quenching effect from a non-protonated amine to the benzene chromophore. This effect is greater for macrocycles in which the first deprotonated amine group is closer to the…

Alkylumlagerungen und acidolyse der ethylidenbrücken bei der synthese von ethylidendiphenolen

1990

For the synthesis of symmetrical and unsymmetrical ethylidenediphenols the corresponding hydroxyphenylethanols (1a–c) were prepared by hydrogenation of hydroxyphenyl methyl ketones with hydrogen/Raney nickle or with lithium aluminium hydride. Condensations of the hydroxyphenylethanols with different phenols under the usual acidic conditions gave products formally resulting form transalkylations. Only the reaction of 1-(3-bromo-2-hydroxy-5-methylphenyl)ethanol (1c) with p-cresol gave the expected product 2d with 82% yield. Experiments with ethylidenediphenols showed that with acids in presence or absence of phenols cleavage and recondensations take place leading to products of formal transal…

Potential use of pulsed electric technologies and ultrasounds to improve the recovery of high-added value compounds from blackberries

2015

Abstract A better knowledge of the effect of non-conventional extraction technologies, which can avoid the use of high temperatures and toxic solvents, on the antioxidant compounds recovery from blackberries, is necessary. Thus, high voltage electrical discharges (HVED), pulsed electric fields (PEF), and ultrasounds (USN) treatments were applied in order to evaluate the effects of processing on protein, total phenolics and anthocyanins extraction from blackberries. Moreover, two-stage extraction involving the use of HVED, PEF and USN as pre-treatments and supplementary extraction during 5 h with hot water at mild temperature (50 °C) or an hydroalcoholic solution (30% ethanol, w/w) was evalu…

Selective oxidative dehydrogenation of ethane on MoVTeNbO mixed metal oxide catalysts

2004

Abstract MoVTeNbO catalysts, prepared by hydrothermal synthesis, are active and highly selective in the ODH of ethane, especially those with a MoVTeNb molar ratio of 1–0.15–0.16–0.17 and heat-treated at 600–650 °C. On the best catalyst, selectivities higher than 80% at ethane conversion levels higher than 80% have been obtained operating at relatively low reaction temperatures (340–400 °C). Thus, yields of ethylene of ca. 75% have been obtained, which exceeds the best yield reported in the literature. Te 2 M 20 O 57 ( M =Mo, V, Nb) and (V,Nb)-substituted θ -Mo 5 O 14 , in addition to small amounts of the Te 0.33 M O 3.33 ( M =Mo, V, Nb) phase, can be proposed in the most selective cataly…

Micellar fluorescence enhancement of carbamate pesticides

1990

Abstract Different studies have been carried out on the interaction of carbamate pesticides, such as carbofuran and carbaryl, with nonionic and anionic surfactants. Micellar fluorescence enhancements (MEF) of 15–20 for carbofuran in the presence of fatty alcohol ethylene oxide condensates, and of 3.7–8.6 in the presence of anionic surfactants at neutral pH have been obtained. Carbaryl does not interact with surfactants, but when it is hydrolysed to 1-naphthol, MEF values of the order of 2 are obtained in the presence of nonylphenol ethylene oxide condensates. The experimental parameters have been optimized in order to obtain maximum fluorescence. The mechanisms involved in the fluorescence …

ChemInform Abstract: Cyclocondensation of 6-Acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine with Hydroxylamine and Hydrazine.

2010

The cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine (3) with hydroxylamine or hydrazine leads to 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenylisoxazolo-[5,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4a) and 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenyl-1H-pyrazolo[3,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4b), respectively. In the presence of methanolic hydrogen chloride, 4b undergoes a cleavage of the pyrimidine ring to yield (5-amino-1,2,4-triazol-1-yl)(3,5-dimethylpyrazol-4-yl)phenylmethane (5). The structure determination of the compounds obtained is based on 1H and 13C nmr spectra including NOE measurements.

Cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine with hydroxylamine and hydrazine

1998

The cyclocondensation of 6-acetyl-4,7-dihydro-5-methyl-7-phenyl[1,2,4]triazolo[1,5-a]pyrimidine (3) with hydroxylamine or hydrazine leads to 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenylisoxazolo-[5,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4a) and 3a,4,9,9a-tetrahydro-3,9a-dimethyl-4-phenyl-1H-pyrazolo[3,4-d][1,2,4]triazolo[1,5-a]pyrimidine (4b), respectively. In the presence of methanolic hydrogen chloride, 4b undergoes a cleavage of the pyrimidine ring to yield (5-amino-1,2,4-triazol-1-yl)(3,5-dimethylpyrazol-4-yl)phenylmethane (5). The structure determination of the compounds obtained is based on 1H and 13C nmr spectra including NOE measurements.