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71.
Ricardo A. W. Neves Filho Diana C. B. da Silva-Alves Janaína V. dos Anjos 《合成通讯》2013,43(19):2596-2602
A simple and straightforward synthesis of 3-aryl-5-hydroxyalkyl-1,2,4-oxadiazoles is described. The reaction among arylamidoximes, ethyl glycolate or ethyl lactate, and potassium carbonate in refluxing toluene afforded the desired 1,2,4-oxadiazoles in moderate to good yields. The synthesis has been accomplished in a single step, avoiding protection–deprotection protocols. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications® to view the free supplemental file. 相似文献
72.
Marcel Špulák Zdeněk Novák Karel Palát Jiří Kuneš Jana Pourová Milan Pour 《Tetrahedron》2013,69(6):1705-1711
Contrary to a number of reports, alkylations of the privileged 3,4-dihydroquinazoline scaffold provide N3-alkylated products, and not 4-alkoxyquinazolines. To correctly assign the structure, 13C NMR shifts of the –Z–CHn– (Z=O, N) fragment are necessary; resonances in the 45–55 ppm range are indicative of N3-alkylation. Treatment of 3,4-dihydroquinazoline-4-one with p-TsCl afforded the N3-tosylated compound, whose reaction with an amine yielded the corresponding N3-alkyl derivative. A mechanism corroborated by 15N-labeling involving pyrimidine ring opening and recyclisation is proposed. Finally, the unambiguous preparation of 4-alkoxyquinazolines is described via treatment of 3,4-dihydroquinazoline-4-ones with PCl5 followed by an alkoxide. 相似文献
73.
Jana Strišovská Veronika Drábová Jozef Kuruc 《Journal of Radioanalytical and Nuclear Chemistry》2013,298(2):1179-1183
The present work describes preparation of 239Np tracer from 243Am stock solution and the purification of this solution from ferric cation. The method of the preparation of tracer involves stabilization of Np(IV) by ascorbic acid and ferric nitrate, separation of 239Np from 243Am by extraction chromatography and determination of recoveries of 239Np by means of gamma spectroscopy. We used the commercially available sorbents TEVA®Resin for the 239Np preparation and DGA Resin for 243Am purification. All sorbents were purchased from Eichrom Industries, Inc. The first eluate from the column can be stored for a future preparation of the tracer and fraction with 239Np will be used to monitor radiochemical yield of 237Np. 相似文献
74.
Hana Macková Daniel Horák Eduard Petrovský Jana Kovářová 《Colloid and polymer science》2013,291(1):205-213
To prepare functionalized magnetic polymer particles that are thermally responsive, inverse emulsion copolymerization of N-isopropylacrylamide, N,N′-methylenebisacrylamide and glycidyl acrylate (GA) was investigated in paraffin oil in the presence of γ-Fe2O3 nanoparticles dispersed in a water/glycerol mixture. The resulting polymer particles were characterized regarding the morphology, size, polydispersity, iron content, and the temperature-dependent phase transition using optical microscopy, transmission electron microscopy, scanning electron microscopy, atomic absorption spectroscopy, and differential scanning calorimetry. Magnetic properties were examined using hysteresis loop measurements and by analyzing the magnetic susceptibility with respect to temperature. We have also investigated the influence of the concentration of γ-Fe2O3 and GA in monomers on properties of the particles (morphology, size, and presence of oxirane groups). The particles possessed a hollow structure as a result of phase separation between water/glycerol hydrophilic solvents in the polymerization feed and the forming polymer. Depending on the concentration of γ-Fe2O3 in the monomer phase, the magnetic hollow particles contained 5–24 wt% iron. In water, the particles gradually collapsed when the temperature was raised to 40 °C because the elevated temperature weakened hydration and the PNIPAAm chains gradually became more hydrophobic. 相似文献
75.
Jana Špaková Raschmanová Miroslava Martinková Jozef Gonda Alena Uhríková 《Chemical Papers》2013,67(10):1317-1329
The stereoselective synthesis of sulfamisterin I and its unnatural analogues II and V in their protected form was achieved through a common strategy. The Wittig reaction of aldehydes VIII and IX with the C14 hydrophobic side-chain X served as the key C-C connecting transformation. Subsequent functional group inter-conversions in the coupling products XI and XX completed the total synthesis. 相似文献
76.
Janaína Versiani dos Anjos Rajendra M. Srivastava Silene Carneiro do Nascimento Sebastião J. de Melo 《Journal of carbohydrate chemistry》2013,32(4):258-277
A copper‐catalyzed reaction of propargyl 4,6‐di‐O‐acetyl‐2,3‐dideoxy‐α‐D‐erythro‐hex‐2‐enopyranoside with 3‐(4‐azidophenyl)‐1,2,4‐oxadiazoles gave the corresponding hexenopyranosides bearing an 1,2,4‐oxadiazole subunit in the aglyconic part of the molecule. The same reaction between ethyl 4‐azido‐2,3,4‐trideoxy‐α‐D‐erythro‐hex‐2‐enopyranoside and acetylenic 1,2,4‐oxadiazoles afforded the corresponding hexenopyranosides carrying a triazole and a 1,2,4‐oxadiazole ring at C‐4 of the carbohydrate. Combination of the two sequences gave hexenopyranosides displaying two 1,2,4‐oxadiazole subunits, each one being embedded in the C‐1 and C‐4 frameworks, of the carbohydrate moiety. A simple dihydroxylation reaction of these unsaturated carbohydrates yielded a series of mannopyranosides bearing one or two 1,2,4‐oxadiazole subunits at C‐1 or C‐4. These new compounds were evaluated for their cytotoxic activities against two cell strains: NCI‐H292 (lung carcinoma) and Hep‐2 (larynx carcinoma), some of them presenting impressive cell growth inhibitions. 相似文献
77.
Jitka Daďová Susanne Kümmel Christian Feldmeier Jana Cibulková Dr. Richard Pažout Dr. Jaroslav Maixner Prof. Dr. Ruth M. Gschwind Prof. Dr. Burkhard König Dr. Radek Cibulka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(3):1066-1075
A series of 10‐arylflavins (10‐phenyl‐, 10‐(2′,6′‐dimethylphenyl)‐, 10‐(2′,6′‐diethylphenyl)‐, 10‐(2′,6′‐diisopropylphenyl)‐, 10‐(2′‐tert‐butylphenyl)‐, and 10‐(2′,6′‐dimethylphenyl)‐3‐methylisoalloxazine ( 2 a – f )) was prepared as potentially nonaggregating flavin photocatalysts. The investigation of their structures in the crystalline phase combined with 1H‐DOSY NMR spectroscopic experiments in CD3CN, CD3CN/D2O (1:1), and D2O confirm the decreased ability of 10‐arylflavins 2 to form aggregates relative to tetra‐O‐acetyl riboflavin ( 1 ). 10‐Arylflavins 2 a – d do not interact by π–π interactions, which are restricted by the 10‐phenyl ring oriented perpendicularly to the isoalloxazine skeleton. On the other hand, N3? H???O hydrogen bonds were detected in their crystal structures. In the structure of 10‐aryl‐3‐methylflavin ( 2 f ) with a substituted N3 position, weak C? H???O bonds and weak π–π interactions were found. 10‐Arylflavins 2 were tested as photoredox catalysts for the aerial oxidation of 4‐methoxybenzyl alcohol to the corresponding aldehyde (model reaction), thus showing higher efficiency relative to 1 . The quantum yields of 4‐methoxybenzyl alcohol oxidation reactions mediated by arylflavins 2 were higher by almost one order of magnitude relative to values in the presence of 1 . 相似文献
78.
Jana Balintová Medard Plucnara Pavlína Vidláková Dr. Radek Pohl Dr. Luděk Havran Prof. Dr. Miroslav Fojta Prof. Dr. Michal Hocek 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(38):12720-12731
Benzofurazane has been attached to nucleosides and dNTPs, either directly or through an acetylene linker, as a new redox label for electrochemical analysis of nucleotide sequences. Primer extension incorporation of the benzofurazane‐modified dNTPs by polymerases has been developed for the construction of labeled oligonucleotide probes. In combination with nitrophenyl and aminophenyl labels, we have successfully developed a three‐potential coding of DNA bases and have explored the relevant electrochemical potentials. The combination of benzofurazane and nitrophenyl reducible labels has proved to be excellent for ratiometric analysis of nucleotide sequences and is suitable for bioanalytical applications. 相似文献
79.
80.
Interactions between CdTe quantum dots and DNA revealed by capillary electrophoresis with laser‐induced fluorescence detection
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Maja Stanisavljevic Jana Chomoucka Simona Dostalova Sona Krizkova Marketa Vaculovicova Vojtech Adam Rene Kizek 《Electrophoresis》2014,35(18):2587-2592
Quantum dots (QDs) are one of the most promising nanomaterials, due to their size‐dependent characteristics as well as easily controllable size during the synthesis process. They are promising label material and their interaction with biomolecules is of great interest for science. In this study, CdTe QDs were synthesized under optimal conditions for 2 nm size. Characterization and verification of QDs synthesis procedure were done by fluorimetric method and with CE. Afterwards, QDs interaction with chicken genomic DNA and 500 bpDNA fragment was observed employing CE‐LIF and gel electrophoresis. Performed interaction relies on possible matching between size of QDs and major groove of the DNA, which is approximately 2.1 nm. 相似文献