Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Yкраїнський (UK)
Przejdź do strony domowej biblioteki Centralna Biblioteka Wojskowa Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaCentralna Biblioteka Wojskowa

Wyszukujesz frazę "Triazole" wg kryterium: Temat

  Lista filtrów
Wyrównaj
Wyświetlanie 1-15 z 38
Tytuł:
Synthesis, characterization and biological property of 3-(5-bromothiophen-2-yl)-6-phenyl-1,7a-dihydro-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole derivatives
Autorzy:
Joshi, Harsh H.
Parsania, M. V.
Powiązania:
https://bibliotekanauki.pl/articles/1075472.pdf
Data publikacji:
2019
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
antibacterial
thiadiazole
triazole
Opis:
A library of novel 3-(5-bromothiophen-2-yl)-6-phenyl-1,7a-dihydro-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole were synthesized in excellent yields via domino one-pot two component reactions of 4-amino-3-(5-bromothiophen-2-yl)-4,5-dihydro-1H-1,2,4-triazole-5-thiol and benzoic acid derivatives respectively. A triazolo-thiadiazole system may be viewed as a cyclic analogue of two very important components - thiosemicarbazide and biguanide which often display diverse biological activities. The significant advantages of this reaction include one-pot process, simple work-up procedure, excellent yields and no column chromatographic purification. All intermediates and final compounds were confirmed by 1H NMR, 13C NMR, Mass Spectroscopy methods and IR analysis.
Źródło:
World Scientific News; 2019, 126; 291-298
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis of 1,2,3-triazole derivative at 3rd position of coumarin via copper(I) catalyzed click chemistry using ternary solvent system (DMF + t-BuOH + water)
Autorzy:
Safi, Shahrukhkhan
Dhamsaniya, Ashish
Christian, Wilson
Trivedi, Prachi
Chhatbar, Pratiksha
Shah, Anamik
Powiązania:
https://bibliotekanauki.pl/articles/1059512.pdf
Data publikacji:
2019
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
Click Chemistry
Coumarin
Triazole
heterocyclic hybrids
Opis:
Coumarin-based triazoles were synthesized from 2-azido-N-phenylacetamide and terminal acetylenic compound by click chemistry. Whereas the CuSO4 used catalyts and sodium ascorbate used as a reducant affords only the favourable 1,4-regioisomer of triazole. Here DMF + t-BuOH + water used as a solvent.
Źródło:
World Scientific News; 2019, 128, 2; 255-301
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and biological activity of pyrazole and 1,2,3-triazole containing heterocyclic compounds
Autorzy:
Bhola, Yogesh
Naliapara, Ashutosh
Modi, Jigna
Naliapara, Yogesh
Powiązania:
https://bibliotekanauki.pl/articles/1076027.pdf
Data publikacji:
2019
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
XRD crystal
antibacterial
azides
hydrazones
pyrazol
triazole
Opis:
As heterocyclic compounds show good biological activity, we have synthesized nitrogen containing compounds among them 9a, 9c, 9e and 9f have shown very good antimicrobial activity with remarkable inhibition zones. N'-((5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methylene)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carbohydrazide (9a-i, 10) was synthesized from 5-(aryloxy)-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde and 5-methyl-1-phenyl-1H-1,2,3-triazole-4-carbohydrazide by condensation in acidic media. 5-(aryloxy)-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde and 5-methyl-1-phenyl-1H-1,2,3-triazole-4-carbohydrazide were synthesized from phenyl hydrazine and substituted anilines respectively. All intermediates and final compounds were confirmed by 1H-NMR, 13C-NMR, Mass Spectroscopy methods and compound 9c was confirmed by single XRD analysis.
Źródło:
World Scientific News; 2019, 117; 29-43
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Triazolo derivatives: Synthesis and ultrasonic behaviour in DMF and DMSO solutions over a wide range of temperatures
Autorzy:
Baluja, Shipra
Pithiya, Mona
Hirapara, Asmita
Lava, Divyata
Powiązania:
https://bibliotekanauki.pl/articles/1158749.pdf
Data publikacji:
2018
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
DMF
DMSO
Triazole
acoustical parameters
ultrasonic velocity
Opis:
Ultrasonic velocity, density and viscosity of two new triazolo derivatives were measured in DMF and DMSO over a range of temperatures. From these measured experimental data, various acoustical parameters were calculated to understand the molecular interactions occurring in the solution.
Źródło:
World Scientific News; 2018, 114; 177-194
2392-2192
Pojawia się w:
World Scientific News
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and Characterization of 1-(1-chlorocyclopropyl)-2-(1,2,4-triazol-1-yl)ethan-1-one
Autorzy:
Ji, H.
Niu, Y.
Liu, D.
Wang, W.
Dai, C.
Powiązania:
https://bibliotekanauki.pl/articles/778677.pdf
Data publikacji:
2017
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
prothioconazole
1,2,4-triazole
N-alkylation reaction
Opis:
A simple and efficient method to prepare 1-(1-chlorocyclopropyl)-2-(1,2,4-triazol-1-yl)ethan-1-one via nucleophilic substitution of 2-chloro-1-(1-chlorocyclopropyl)ethanone and 1,2,4-triazole is described. The title compound is the key intermediate required for the synthesis of prothioconazole, a promising agricultural fungicide. By exploring changes in the reaction time, temperature, ratio of starting reagents, acid binding agent, and the nature of phase transfer catalyst, the reaction conditions could be optimized to afford the desired N-alkylated material in near-quantitative yield. The ultimate yield of the product after recrystallization was 93%, with a purity of 99% based on its characterization by Gas Chromatography-Mass Spectrometer (GC-MS), Fourier Transform infrared spectroscopy (IR), Proton Magnetic Resonance (1H NMR), and Carbon-13 Nuclear Magnetic Resonance (13C NMR). The synthetic process is suitable for industrial application, with the advantages of high yield and facile preparation under mild operating conditions.
Źródło:
Polish Journal of Chemical Technology; 2017, 19, 1; 41-47
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Design, Efficient Synthesis, Mechanism of Reaction and Antiproliferative Activity Against Cancer And Normal Cell Lines of A Novel Class of Fused Pyrimidine Derivatives
Autorzy:
roaiah, hanaa F.
Rashdan, Huda R.
soliman, abdelmohsen
Muhammed, Zeinab
Wietrzyk, Joanna
Milczarek, Magdalena
Powiązania:
https://bibliotekanauki.pl/articles/895705.pdf
Data publikacji:
2018-06-30
Wydawca:
Polskie Towarzystwo Farmaceutyczne
Tematy:
anticancer activity
antiproliferative activity
Coumarin
Fused pyrimidines
3-triazole
Opis:
This work concentrated on the utility of hydrazonoyl halides in synthesis of bioactive heterocycles like triazoles, pyrazoles, pyrimidines and their fused derivatives which have a wide spectrum of pharmaceutical value. Herein we discussed the synthesis of new heterocyclic compounds containing fused pyrimidine rings derived from hydrazonoyl halides and their significant pharmaceutical importance as anticancer agents. New fused pyrimidine derivatives bearing 1,2,3-triazole moiety were prepared via reaction of enaminone 2 with and 6-amino-2-thioxo-pyrimidin-4-one and then with hydrazonoyl chlorides 6a-h. In addition 3-amino-6-(2-oxo-2H-chromen-3-yl)pyridine-2-carbonitrile (12) was submitted to react with carbon dioxide to afford 3-(1,2,3,4-tetrahydro-2,4-dithioxopyrido[2,3-d]pyrimidin-7-yl)-2H-chromen-2-one (15), which act as key molecule for synthesis of new series of fused prymidinethione derivatives containing coumarine moiety via its reaction with different selected derivatives of hydrazonoyl halides 6a-h. Structures of the newly synthesized compounds were confirmed using spectral data (IR, H1NMR and Mass spectrometry) and microanalytical methods. Also, they screened for their anticancer activity.
Źródło:
Acta Poloniae Pharmaceutica - Drug Research; 2018, 75, 3
0001-6837
2353-5288
Pojawia się w:
Acta Poloniae Pharmaceutica - Drug Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and biological activity of 1,2,4-triazolo-[3,4-b]thiadiazole as antimicrobial agents
Autorzy:
Vekariya, P. B.
Pandya, J. R.
Goswami, V.
Joshi, H. S.
Powiązania:
https://bibliotekanauki.pl/articles/412334.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
6-Fluoro chroman
1,2,4-triazole
triazolothiadiazole
antimicrobial activity
Opis:
Some novel 6-fluoro chroman derivatives having 1,2,4-triazolo-[3,4-b]thiadiazole were synthesized and characterized by IR, NMR and mass spectral analysis. All synthesized compounds were screened for antimicrobial activity using broth dilution method. All the compounds showed good antimicrobial activity and compound 5e showed significant antibacterial activity.
Źródło:
International Letters of Chemistry, Physics and Astronomy; 2014, 7; 45-52
2299-3843
Pojawia się w:
International Letters of Chemistry, Physics and Astronomy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Relation of the polymorphism of cyp51A sequence and the susceptibility of Aspergillus fumigatus isolates to triazoles determined by commercial gradient test (Etest) and by reference methods
Autorzy:
Nawrot, Urszula
Sulik-Tyszka, Beata
Kurzyk, Ewelina
Mroczyńska, Martyna
Włodarczyk, Katarzyna
Wróblewska, Marta
Basak, Grzegorz
Brillowska-Dąbrowska, Anna
Powiązania:
https://bibliotekanauki.pl/articles/1038548.pdf
Data publikacji:
2017
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
Aspergillus fumigatus
triazole resistance
susceptibility testing
Etest
cyp51A sequence
Opis:
The aim of this study was to evaluate the accuracy of commercial gradient test (Etest) in the detection of triazole resistant Aspergillus fumigatus isolates using reference microdilution methods and the analysis of sequences of the cyp 51A gene. The study was performed on twenty clinical isolates which were identified as Aspergillus fumigatus based on the DNA sequences of the ITS1-2 fragment of ribosomal DNA and the β-tubulin gene, out of them seventeen isolates showed wild-type cyp51A sequence and three were positive for the mutation TR34/L98H. All isolates were tested for the susceptibility to itraconazole (ITZ), voriconazole (VOR) and posaconasole (POS) using microdilution methods, according to EUCAST and CLSI protocols, as well as using Etest. The results of microdilution and Etests were analysed separately according to clinical breakpoints (CBP) defined by EUCAST version 7.0 and epidemiological cut off values (ECV). Etest as well as reference methods excellently recognised the WT isolates, which were susceptible to all tested triazoles, regardless of the method and CBP or ECV criteria used. The Etest recognized three non-WT isolates as resistant or intermediately sensitive to ITZ and POS and one as resistant to VOR. The categorical concordance between Etests and EUCAST and Etests and the CLSI method ranged from 90 to 100%. The interpretation of the results obtained from routine A. fumigatus Etests requires great caution. The use of the confirmative examinations with reference AST methods as well as with molecular tests is recommended.
Źródło:
Acta Biochimica Polonica; 2017, 64, 4; 631-634
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Synthesis and antimicrobal activities of some novel triazolo[1,5-a]pyrimidine derivatives
Autorzy:
Gami, S. P.
Vilapara, K. V.
Khunt, H. R.
Babariya, J. S.
Naliapara, Y. T.
Powiązania:
https://bibliotekanauki.pl/articles/412170.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
5-amino-1,2,4-triazole
ketene dithioacetal
antimicrobial activity
triazolopyrimidine
Opis:
A convenient synthesis of substituted 1,2,4-triazolo[1,5-a]pyrimidine was carried out by the reaction of various ketene dithioacetals with 5-amino 1,2,4-triazole in methanol in presence of sodium methoxide. The newly synthesized compound were characterized by 1H NMR, 13C NMR, IR, MS, elemental analysis and screened for their antimicrobial activity against various strains of bacteria and fungi.
Źródło:
International Letters of Chemistry, Physics and Astronomy; 2014, 11, 2; 127-134
2299-3843
Pojawia się w:
International Letters of Chemistry, Physics and Astronomy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Acetylation of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate
Autorzy:
Dżygiel, Anetta
MAsiukiewicz, Elżbieta
Rzeszotarska, Barbara
Powiązania:
https://bibliotekanauki.pl/articles/1044073.pdf
Data publikacji:
2001
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
hetareneamino acid
5-amino-1H-[1,2,4]triazole-3-carboxylate
Opis:
Acetylation with acetic anhydride of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate, one of the hetareneamino acids, was studied using HPLC,1H NMR, FTIR and GC-MS. The compound has a significantly decreased susceptibility to acetylation compared to 5-amino-1H-[1,2,4]triazole itself. Two isomeric diacetylated products were found.
Źródło:
Acta Biochimica Polonica; 2001, 48, 4; 1169-1173
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Melt-cast Energetic Matrices with 3-Nitro-1,2,4-triazole Derivatives for Composite Explosives
Autorzy:
Komarova, Marina
Vakutin, Aleksey
Kazutin, Maxim
Kozyrev, Nikolai
Sukhanov, Gennady
Powiązania:
https://bibliotekanauki.pl/articles/1063044.pdf
Data publikacji:
2020
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
melt-cast energetic matrix
3-nitro-1,2,4-triazole
TNT
composite explosives
Opis:
Safety requirements for the manufacture, use and storage of high-energy materials and explosive substances necessitate a search for new insensitive components of fusible energetic matrices (propellant matrices) in order to completely or partially replace 2,4,6-trinitrotoluene (TNT). 3-Nitro-1,2,4-triazole derivatives and their melt-casts with TNT may be proposed as such replacements. Differential scanning calorimetry was employed to characterize the thermal behaviour of 1-methyl-3-nitro-1,2,4-triazole, 1-ethoxymethyl-3-nitro-1,2,4-triazole, t-butyl-3-nitro-1,2,4-triazole and their melt-casts with TNT. This study showed that 1-methyl-3-nitro-1,2,4-triazole and its melt-casts with TNT was the best for explosive systems based on 2,4,6,8,10,12-hexanitro-1,4,6,8,10,12-hexaazaisowurtzitane (HNIW), 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane (HMX) and guanylurea dinitramide (GUDN). The present article also presents data for the mechanical sensitivity of these explosives and their calculated detonation characteristics. The composite explosive based on HMX with 1-methyl-3-nitro-1,2,4-triazole has a calculated detonation velocity the same as HMX with TNT, but the sensitivity of HMX/TNT is 1.3-1.7 times higher.
Źródło:
Central European Journal of Energetic Materials; 2020, 17, 3; 344-361
1733-7178
Pojawia się w:
Central European Journal of Energetic Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Detonation and Decomposition Characteristics of Dichlorate(VII) μ-Tris(4-amino-1,2,4-triazole)copper(II)
Autorzy:
Cudziło, S.
Trzciński, W. A.
Paszula, J.
Nita, M.
Powiązania:
https://bibliotekanauki.pl/articles/358059.pdf
Data publikacji:
2014
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
4-amino-1,2,4-triazole
complex copper compound
primary explosive
detonation parameters
Opis:
Dichlorate(VII) μ-tris(4-amino-1,2,4-triazole)copper(II) is an explosive with a performance close to that of lead azide. However, it is quite stable and has moderate sensitivity to thermal and mechanical stimuli. In order to fully characterize it as a primary explosive, its thermal decomposition kinetics were studied and some important detonation and explosion parameters (detonation heat and velocity, acceleration ability, water shock wave overpressure, and energy) were measured and/or calculated.
Źródło:
Central European Journal of Energetic Materials; 2014, 11, 4; 539-552
1733-7178
Pojawia się w:
Central European Journal of Energetic Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Wyświetlanie 1-15 z 38

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies