共查询到20条相似文献,搜索用时 46 毫秒
1.
Robert Musiol Josef Jampilek Barbara Podeszwa Jacek Finster Dominik Tabak Jiri Dohnal Jaroslaw Polanski 《Central European Journal of Chemistry》2009,7(3):586-597
In the present paper we describe results on the synthesis and lipophilicity determination of a series of biologically active
compounds based on their heterocyclic structure. For synthesis of styrylquinoline-based compounds we applied microwave irradiation
and solid phase techniques. The correlation between RP-HPLC retention parameter log k (the logarithm of retention factor k) and log P data calculated in various ways is discussed, as well as, the relationships between the lipophilicity and the chemical structure
of the studied compounds.
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Dominique R. Duguay Matthew T. Zamora Johanna M. Blacquiere Francis E. Appoh Christopher M. Vogels Susan L. Wheaton Felix J. Baerlocher Andreas Decken Stephen A. Westcott 《Central European Journal of Chemistry》2008,6(4):562-568
The addition of formylphenylboronic acid derivatives to thiourea and ethyl acetoacetate proceeds in the presence of an additional
Lewis acid catalyst to give the corresponding 3,4-dihydropyrimidin-2(1H)-(thio)ones (Biginelli products) in moderate yield.
Compounds were tested for antifungal activity against pure cultures of Aspergillus niger, Aspergillus flavus, Candida albicans and Saccharomyces cerevisiae but, unfortunately, none showed any appreciable activity.
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The reaction mechanism between AlX and HX (X = Br, Cl, and F) have been characterized in detail using DFT as well as the ab initio method. The reaction yielding AlX3 and molecular hydrogen was calculated to be highly exothermic. The present calculations also show that the possible routes
to the trihalides species start more favorable with the primary insertion product AlX2H than with the biadduct AlX(HX)2 one.
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7.
Santosh S. Katkar Pravinkumar H. Mohite Lakshman S. Gadekar Balasaheb R. Arbad Machhindra K. Lande 《Central European Journal of Chemistry》2010,8(2):320-325
A rapid and an efficient one-pot method for the synthesis of quinoxalines catalysed by ZnO-beta zeolite at room temperature
is described. This environmentally benign method provides several advantages over methods that are currently employed such
as a simple work-up, mild reaction conditions, good to excellent yields, and a process to recover and reuse the catalyst for
several cycles with consistent activity.
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8.
Cory C. Pye 《Central European Journal of Chemistry》2011,9(4):567-571
A geometry and SCF convergence study of Hartree-Fock calculations using the 6-31G* basis set is carried out on the set of
all possible diatomic molecules formed from atoms with Z≤36. The utility of Hartree-Fock calculations using the smaller STO-3G
basis set to improve the convergence behavior is demonstrated.
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9.
Phase equilibria established in the PbO - BiVO4 system over the whole component concentration range up to 1000°C have been investigated. A phase diagram has been constructed
using DTA and XRD.
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10.
Renata Farkas Mercedesz Törincsi Pal Kolonits Jenö Fekete Oscar Jimenez Alonso Lajos Novak 《Central European Journal of Chemistry》2010,8(2):300-307
During the diazo-coupling reaction, nucleophilic displacement of a nitro group was also observed. This was the main reaction
(1→7) when the starting amine bore either a chlorine or methoxy group at the para position (1b–c). The newly prepared compounds (7) might serve as convenient building blocks in synthesis of some heterocycles.
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11.
Tsonko Kolev Bojidarka B. Koleva Michael Spiteller 《Central European Journal of Chemistry》2008,6(3):393-399
The applications of linear-polarized IR-spectroscopy to oriented colloid suspensions in a nematic host are demonstrated with
croconic and rhodizonic acids. The experimental IR vibrational assignments of the solid-state of both neutral compounds are
presented. Assignments are supported by theoretical quantum chemical calculations and vibrational analysis at the DFT level
of theoretical approximation with the 6-311++G** basis set.
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12.
Vendula Houšková Václav Štengl Snejana Bakardjieva Nataliya Murafa Václav Tyrpekl 《Central European Journal of Chemistry》2009,7(2):259-266
Nanocrystalline titania particles doped with ruthenium oxide have been prepared by the homogenous hydrolysis of TiOSO4 in aqueous solutions in the presence of urea. The synthesized particles were characterized by X-ray diffraction (XRD), Scanning
Electron Microscopy (SEM), High Resolution Transmission Electron Microscopy (HRTEM), Selected Area Electron Diffraction (SAED)
and Nitrogen adsorption-desorption was used for surface area (BET) and porosity determination (BJH). The photocatalytic activity
of the Ru-doped titania samples were determined by photocatalytic decomposition of Orange II dye in an aqueous slurry during
irradiation at 365 nm and 400 nm wavelengths.
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13.
Nitin A. Mirgane Sandip B. Kotwal Anil V. Karnik 《Central European Journal of Chemistry》2010,8(2):356-360
Ionic liquids (IL) are gaining importance as green solvents. Imidazolium ionic liquid [bmim]+[Cl]−, an environmentally benign solvent, was found to promote the Diels-Alder reaction between anthrone and maleimides at room
temperature with excellent yields. The ionic liquid played a dual role as solvent and catalyst.
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14.
The triplet excited state properties and photosensitization mechanisms of indigo were investigated based on density functional
theory calculations. The solvent effects on the photosensitization mechanisms of indigo have also been considered. The thermodynamic
feasibility of the possible 1O2 and O2·−-photogeneration pathways by triplet excited state indigo in different solvents was explored, in order to gain some deeper
insights into the photosensitization characters of the dye.
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Vivek Srivastava 《Central European Journal of Chemistry》2010,8(2):269-272
Sulphonimide based organocatalyst was used to catalyze the aldol reaction in ionic liquid media. On the basis of yield and
selectivity the ionic liquid mediated system was found superior in comparison with organic solvents. The added advantages
of this ionic liquid mediated organocatalysis are easy recovery of product and the recyclability of the organocatalyst.
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16.
Tuula Kylmälä Jan Tois Youjun Xu Robert Franzén 《Central European Journal of Chemistry》2009,7(4):818-826
Diflunisal and Felbinac, two FDA-approved NSAIDs and other biphenyl carboxylic acids were prepared in one step by a simple
and clean Suzuki cross-coupling reaction using an easily synthesized, air and moisture stable, palladium-diamine complex.
The yield (93%) for the one-step preparation of Diflunisal is the best reported without using a glovebox and a phoshine-based
catalyst.
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17.
Lakshman S. Gadekar Shivshankar R. Mane Santosh S. Katkar Balasaheb R. Arbad Machhindra K. Lande 《Central European Journal of Chemistry》2009,7(3):550-554
Natural scolecite has been found as an effective catalyst for the one-pot synthesis of 2,4,5-triarylimidazole derivatives
via a three component reaction using benzil or benzoin, aldehydes and ammonium acetate. This method provides several advantages
such as being environmentally benign, reusable, possessing high yields with increased variations of the substituents in the
product and preparative simplicity.
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18.
The oxidation processes of 2,6-diisopropylnaphthalene and 4,4′-diisopropylbiphenyl with oxygen in the presence of a catalyst,
composed of copper(II) chloride and tetrabutylammonium bromide, were investigated. It was found that, in essence, only one
isopropyl group undergoes oxidation, and obtained mixtures contained mainly peroxide, alcohol, ketone and only small amounts
of hydroperoxide.
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19.
Anuţa Câmpean Mihaela Tertiş Robert Săndulescu 《Central European Journal of Chemistry》2011,9(4):688-700
Electrochemical behaviour of some alkaloids, namely: caffeine, aminophylline, theophylline, codeine phosphate and papaverine
hydrochloride, that are in solution in various combinations or in the presence of other compounds contained in pharmaceuticals
or in real samples (urine) was investigated using cyclic voltammetry (CV), square-wave voltammetry (SWV) and differential
pulse voltammetry (DPV) on electrochemically activated glassy carbon electrode.
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20.
A novel hydroxyamino phosphane was synthesised through the reaction of 2-imidazolidinone with ClPPh2 and subsequently reaction
of the resulting bisphosphino derivative with the Grignard reagent BrMgC5H11. The interaction of the pentyl substituent with one of the two phosphino groups and the structure in solution is shown by
multinuclear NMR-spectroscopy..
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