共查询到20条相似文献,搜索用时 31 毫秒
1.
Jekaterina Rjabova Vitālijs Rjabovs Antonio J. Moreno Vargas Elena Moreno Clavijo Māris Turks 《Central European Journal of Chemistry》2012,10(2):386-394
Recently, monosaccharide-triazole conjugates have proved to possess a large variety of useful biological activities. This
paper describes synthesis of a new series of 3-deoxy-3-C-triazolylmethyl-allose derivatives. These new compounds are obtained from acetonide-protected 3-deoxy-3-azidomethyl allose
and commercial alkynes via Cu(I) catalyzed 1,3-dipolar cycloaddition. The obtained molecular scaffolds differ from those described
earlier by the presence of a methylene linker (-CH2-) between the C(3) of allose and the triazole moiety. It was demonstrated that acetonide-protected monosaccharide, 3-deoxy-3-C-(4-phenyl-1H-1,2,3-triazol-1-yl)methyl-1,2:5,6-di-O-isopropylidene-α-d-allofuranose, inhibited α-L-fucosidase for 26% at 0.1 mM concentration, but a deprotected analog, 3-deoxy-3-C-(4-(4-tert-butylphenyl)-1H-1,2,3-triazol-1-yl)methyl-β-d-allofuranose, showed 15% inhibition of β-glucosidase at 1 mM concentration.
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2.
Yu. L. Zborovskii V. V. Orysyk V. I. Staninets V. V. Bon’ 《Russian Journal of Organic Chemistry》2011,47(6):881-885
Cyclization of 2-(2-{4-[allylamino(thioxo)methyl]piperazin-1-yl}ethyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione by the action of iodine, bromine, or sulfuryl chloride gave 2-(2-{4-[4,5-dihydro-5-(halomethyl)-thiazol-2-yl]piperazin-1-yl}ethyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione hydrohalides which were converted into 2-{2-[4-(5-methylthiazol-2-yl)piperazin-1-yl]ethyl}-1H-benzo[de]isoquinoline-1,3(2H)-dione. 相似文献
3.
Saravanakumar Shanmuganathan Olaf Kühl Peter G. Jones Joachim Heinicke 《Central European Journal of Chemistry》2010,8(5):992-998
The reaction of chloroethyltrimethylsilylether with 1-methylimidazole furnishes an ionic liquid that undergoes methanolysis
to crystalline 2-hydroxyethylimidazolium chloride (crystal structure presented). Conversion to defined hydroxyethylimidazol-2-ylidene
nickel complexes failed, but was accomplished with 1-methyl-3-acetophenyl-imidazolium bromide. The bis(NHC⋂O−) nickel(II) chelate is formed, rather than a methallylnickel monochelate, but with nickelocene a monochelate NiCp complex
was detected. The bulky 1-(2,6-diisopropylphenyl)-3-(2’-phenyl-enolato)-imidazol-2-ylidene allylpalladium chloride was obtained
in pure form. Attempts to generate catalysts for ethylene oligomerization by in situ techniques have failed so far whereas P⋂O− ligands, comparable by the P-C diagonal relationship, provide active catalysts.
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4.
Agata Siwek Monika Wujec Maria Dobosz Ewa Jagiełło-Wójtowicz Anna Chodkowska Agnieszka Kleinrok Piotr Paneth 《Central European Journal of Chemistry》2008,6(1):47-53
By the reaction of 2-methyl-furan-3-carboxylic acid hydrazide with isothiocyanates, 1-[(2-methyl-furan-3-yl)carbonyl]-4-substituted
thiosemicarbazides 1 were obtained. Further cyclization with 2% NaOH led to the formation of 3-(2-methyl-furan-3-yl)-4-substituted-Δ2-1,2,4-triazoline-5-thiones 2. The pharmacological effects of 2 on the central nervous system in mice were investigated. Strong antinociceptive properties
of the investigated derivatives were observed in a wide range of doses.
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5.
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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6.
Vasile-Nicolae Bercean Valentin Badea Călin Deleanu Alina Nicolescu 《Central European Journal of Chemistry》2012,10(2):373-379
1H-1-Alkyl-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles (2aa-ad) were obtained by regioselective alkylation of 1H-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles (2a). 1H-1-Alkyl-6-methyl-3-phenyl-7-phenylazopyrazolo[5,1-c][1,2,4]triazoles 2aa and 2ab were also prepared by coupling phenyldiazonium chloride with 1H-1-alkyl-6-methyl-3-phenyl-pyrazolo[5,1-c][1,2,4]triazoles 1aa and 1ab. The new compounds were characterized by IR, UV-VIS, 1H-NMR, 13C-NMR, and 15N-NMR spectroscopy and their structures and actual tautomeric forms were established unequivocally.
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7.
The present work reports the synthesis, characterization and performance of a new zinc(II) complex of [Zn(C3H7-bim)2Br2] (bim = benzimidazole) as electrocatalyst for trichloroacetic acid and bromate reduction. Its structure was characterized
by X-ray crystallography, IR spectroscopy and elemental analysis. The zinc atom adopts a distorted tetrahedral geometry by
coordinating to two bromine atoms and two nitrogen atoms from two 1-propyl-1H-benzo[d]imidazole ligands. The electrochemical behavior and electrocatalysis of the zinc complex bulk-modified carbon paste electrode
(Zn-CPE) have been studied by cyclic voltammetry. The Zn-CPE shows good electrocatalytic activities toward the reduction of
trichloroacetic acid and bromate. The detection limit and the sensitivity are 0.05 μM, 67.43 μA μM−1 for trichloroacetic acid detection, and 0.02 μM, 69.94 μA μM−1 for bromate detection, respectively. This modified electrode shows good reproducibility, high stability, low detection limit,
technical simplicity and possibility of rapid preparation, which is important for practical applications.
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8.
Sergey Zhersh Oleksandr V. Karpenko Vasyl Ripenko Andrey A. Tolmachev Oleksandr O. Grygorenko 《Central European Journal of Chemistry》2014,12(1):67-73
A convenient preparation of 1-(pyrrolidin-2-yl)-1H-pyrazoles, -imidazoles, and -1H-1,2,4-triazoles, 1-(piperidin-2-yl)-1H-pyrazoles and -1H-1,2,4-triazoles, and 1-(piperidin-3-yl)-1H-1,2,4-triazoles by alkylation of azoles (viz. pyrazoles, imidazoles, and triazoles) with N-Cbz-prolinol mesylate or its analogues and subsequent deprotection is reported. The two-step method allows for synthesis of the title compounds in 16–65% yields. The utility of the procedure has been demonstrated by multigram preparation of a 15-member building block mini-library for the lead-oriented synthesis of compound libraries. These building blocks perfectly fit the definition of low-molecular-weight hydrophilic three-dimensional templates, which leave much room for the lead-oriented synthesis of the compound libraries. 相似文献
9.
Jorge Luis Sague Doimeadios 《Central European Journal of Chemistry》2008,6(4):505-508
Herein, the first example of a co-crystal system formed by an imidazolium nitrate, a carbene precursor, and copper (II) nitrate,
{[Cu(NO3)2(H2O)2]L1(NO3)2} (1) (L1 = 1,1′-dibenzyl-3,3′-butyl-diimidazolium-2,2′-diylidene) is reported. These two building blocks are connected in the solid
state through hydrogen bonds to generate a three-dimensional supramolecular network.
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10.
Waleed Azzam 《Central European Journal of Chemistry》2009,7(4):884-899
Self-assembled monolayers (SAMs) of ω-(4′-methylbiphenyl-4-yl)ethanethiol (CH3(C6H4)2(CH2)2SH, BP2) prepared at different temperatures on Au(111) substrates were investigated using scanning tunneling microscopy (STM).
Also, the effect of the incubation time of the gold substrate in the thiol solution was examined. The STM results showed that
samples prepared at room temperature were significantly different from those prepared at elevated temperatures in their surface
morphology, space group and size of unit cell. The micrographs of samples prepared at higher temperatures revealed a pronounced
and progressive increase in the size of the well-known etch-pits at the expense of their density with increasing preparation
temperature (but the increase did not continue for SAMs prepared at 348 K). The average domain size was found to increase
significantly with increasing preparation temperature. In addition, polymorphism was observed in BP2 SAMs at all investigated
temperatures. This study has demonstrated that solution temperature and incubation time are key factors controlling the two-dimensional
SAM structure of BP2 molecules.
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11.
Mehdi Ghandi Parham Asgari Abuzar Taheri Alireza Abbasi 《Central European Journal of Chemistry》2010,8(4):899-905
One-pot, three-component condensation of 2-hydroxybenzaldehyde derivatives, primary amines with alkyl isocyanides is reported.
N-alkyl-2-(2-hydroxyphenyl)-2-iminoacetamide derivatives are generated presumably via the preliminary formation of N, N′-disubstituted benzo[b]furan-2,3-diamines and subsequent oxidation with molecular oxygen.
相似文献
12.
Khalid A. Al-Farhan Ismail Warad Saud I. Al-Resayes Moustafa M. Fouda Mohamed Ghazzali 《Central European Journal of Chemistry》2010,8(5):1127-1133
Borneol is a monoterpene that is a part of traditional Chinese and Japanese medicine. (−) borneol reacted with methanesulfonyl
chloride in THF/pyridine to afford the new 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate derivative in excellent
yield. The product is characterized by H1NMR, C13NMR, mass spectroscopy as well as elemental analysis and its structure was identified by X-ray single crystal diffraction.
The packing of 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methanesulfonate exhibits the non-classical C-H···O hydrogen bonding
in C(4) and R2
2(8) chain and ring motifs as structural determinants. This was also confirmed by the analysis of Hirshfeld surfaces. The 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl
methane sulfonate antimicrobial activity was tested and compared with its parent (−) borneol against three different pathogens.
Particularly, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate showed high sensitivity, compared to Chloramphenicol
reference material, against Escherichia coli.
相似文献
13.
Sushilkumar A. Jadhav 《Central European Journal of Chemistry》2012,10(5):1640-1646
Two new long-chain carboxylic acids (1, 2) bearing strong fluorescent group pyrene as ligands for Self-Assembled Monolayers (SAMs) have been synthesized. The multistep targeted synthesis is accomplished by use of Pyren-1-yl methylamine hydrochloride and employing simplified synthetic protocols. Compound 2 contains a chiral center purposely introduced along the atom chain in order to make it suitable for chiro-optical studies of the resulting SAMs. 相似文献
14.
U. Ceren Başköse Sevgi Haman Bayarı Semran Sağlam Hacı Özışık 《Central European Journal of Chemistry》2012,10(2):395-406
The conformational analysis of rasagiline [N-propargyl-1(R)-aminoindan] was performed by the density functional theory (DFT) B3LYP method using the 6–31++G (d,p) basis set. A single
point energy calculations based on the B3LYP optimized geometries were also performed at MP2/6-31++G (d, p) level. The vibrational
frequencies of the most stable conformer of rasagiline was calculated at the B3LYP level and vibrational assignments were
made for normal modes on the basis of scaled quantum mechanical force field (SQM) method. The influence of mesylate and ethanedisulfonate
salts on the geometry of rasagiline free base and its normal modes are also discussed.
相似文献
15.
Maria-Gabriela Alexandru Tanja Cirkovic Velickovic Ioana Jitaru Sanja Grguric-Sipka Constantin Draghici 《Central European Journal of Chemistry》2010,8(3):639-645
This paper presents the synthesis of complex compounds of type [M(L1)2], where M(II)= Cu (1), Co (2), Zn (3), L1=2-aminothiazole-4-acetate and [Mn(L1)2(H2O)] (4) using ethyl 2-(2-aminothiazole-4-yl) acetate (L), and characterization by elemental analysis, magnetic susceptibilities,
IR, 1H-NMR, UV-Vis spectroscopy and for [Mn(L1)2(H2O)] also by X-ray diffraction. In vitro cytotoxicity studies were performed on human cervix adenocarcinoma, HeLa cells. The
antitumor selectivity was assessed using normal human peripheral blood mononuclear cells, PBMC as control.
相似文献
16.
Carla Ferragina Romolo Di Rocco Pasquale Patrono Lucantonio Petrilli 《Central European Journal of Chemistry》2009,7(1):31-34
Layered compounds with CdS particles supported on the ion-exchanger, γ-titanium dihydrogen phosphate, were prepared by the
stepwise reaction of the ion-exchanger and cadmium solution, followed by reaction with H2S gas. The CdS content on the ion-exchanger is dependent on the timeframe of the H2S gas flow. The materials obtained were layered, as shown by the X-ray measurements that exhibit both precursor and CdS diffraction
peaks. The thermal treatment of the material obtained gives evidence of its stability (≤ 320°C) before the CdS decomposition,
which occurs in a single step.
相似文献
17.
Li-Wen Xu Ming-Song Yang Jian-Xiong Jiang Hua-Yu Qiu Guo-Qiao Lai 《Central European Journal of Chemistry》2007,5(4):1073-1083
Ionic liquid-functionalized mesoporous materials exhibited high catalytic activity in versatile organic reactions, such as
cycloaddition of carbon dioxide (CO2) with epoxide, aza-Michael addition of amines to α, β-unsaturated carbonyl compounds, and the Biginelli reaction of aldehyde, ethyl acetoacetate and urea. Recycling of the catalyst
in these reactions could be carried out and the catalyst used at least five times without significant loss in activity.
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18.
Ramin Ghorbani-Vaghei Seyedeh Mina Malaekehpour 《Central European Journal of Chemistry》2010,8(5):1086-1089
N,N,N,’N’-Tetrabromobenzene-1,3-disulfonamide [TBBDA] is found to be a reusable catalyst for efficient synthesis of various amidoalkyl
naphthols from β-naphthol, aromatic aldehydes and urea in good to high yields under solvent-free conditions.
相似文献
19.
D. A. Svechkarev G. V. Karpushina L. L. Lukatskaya A. O. Doroshenko 《Central European Journal of Chemistry》2008,6(3):443-449
Three 2-(benzimidazol-2-yl)-3-hydroxychromone derivatives were synthesized. Their spectroscopic and fluorescent properties,
due to excited state intramolecular proton transfer (ESIPT) from OH to carbonyl, were studied. Theoretical possibility of
an alternative intramolecular H-bonding and experimental evidence for such behavior are discussed.
相似文献
20.
Mi?osz Mi?tkiewski Beata Powa?a Bartosz Staniszewski Maciej Kubicki W?odzimierz Urbaniak Cezary Pietraszuk 《Central European Journal of Chemistry》2011,9(4):728-736
Selected β-diketones bearing unsaturated derivatives have been demonstrated to undergo homo-metathesis and cross-metathesis with selected
olefins in the presence of Grubbs catalysts. The reactions led to respective homo- and cross-metathesis products mainly with
good yields and selectivities.
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