Results 191 to 200 of about 37,093 (255)
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Future Medicinal Chemistry, 2019
AIM In recent times, heterocyclic chemotypes are being explored for the development of new antimycobacterials that target the drug-resistant tuberculosis.
Vitthal B. Makane +9 more
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AIM In recent times, heterocyclic chemotypes are being explored for the development of new antimycobacterials that target the drug-resistant tuberculosis.
Vitthal B. Makane +9 more
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ChemInform Abstract: 1,3,4‐Oxadiazole
ChemInform, 2014AbstractReview: use of oxadiazole derivatives in in various field like polymer industry and, ost notably, medicinal chemistry; 70 refs.
S. B. Dave, P. Godhani, Y. Ushir
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Recent Advancement in Synthesis and Bioactivities of 1,3,4-Oxadiazole
Current Organic Synthesis, 2023Abstract: Derivatives of 1,3,4-oxadiazole are effective in the treatment and cure of a wide range of diseases in medical chemistry, while industrial development has shown that they can be utilised as corrosion inhibitors and light-emitting diodes.
Tarun, Chaudhary +1 more
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Novel syntheses of symmetrical 2,5-diaryl-1,3,4-oxadiazoles and 1,4-phenylenebis-1,3,4-oxadiazoles
Russian Chemical Bulletin, 1998The reactions of trichloromethylarenes with excess hydrazine hydrate in ethanol gives symmetrical 2,5-diaryl-1,3,4-oxadiazoles in 68–96% yields. The reaction of 1,4-bis(trichloromethyl)benzene with acylhydrazines in an ethanol-pyridine mixture gives the corresponding substituted or unsubstituted 1,4-phenylenebis-1,3,4-oxadiazoles in 35–51% yields.
L. I. Belen'kii +3 more
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Perfluoro-bis-1,3,4 oxadiazoles
Bulletin of the Academy of Sciences, USSR Division of Chemical Science, 19651. The hydrazides of perfluorodicarboxylic acids of the general formula NH2NHCO(CF2)nCONHNH2 (n= 3,4,8,12) were produced by the action of hydrazine hydrate on the diethyl esters of the perfluorodicarboxylic acids in alcohol solutions. 2.
M. P. Krasuskaya +2 more
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Journal of Molecular Graphics and Modelling, 2019
The mechanism of the reaction of 1,3,4-oxadiazoles with alkenes (ethylene) and cycloalkenes (cyclobutene, cyclopentene, cyclohexene and cycloocene) have been studied computationally at the DFT M06-2X/6-311G* level.
D. Roland +4 more
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The mechanism of the reaction of 1,3,4-oxadiazoles with alkenes (ethylene) and cycloalkenes (cyclobutene, cyclopentene, cyclohexene and cycloocene) have been studied computationally at the DFT M06-2X/6-311G* level.
D. Roland +4 more
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Aliphatic poly‐1,3,4‐oxadiazoles
Journal of Polymer Science Part A: General Papers, 1965AbstractThree high molecular weight aliphatic polyoxadiazoles have been prepared by a new route from equimolar amounts of a diphenyl ester of dicarboxylic acid and an anhydrous hydrazine (or a dihydrazide). The resulting polymers have been characterized by microanalysis, intrinsic viscosity, x‐ray diffraction patterns, infrared absorption spectra, and ...
Terunobu Unishi, Masaki Hasegawa
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Anti-inflammatory Activity of Substituted 1,3,4-Oxadiazoles
Journal of Pharmaceutical Sciences, 1994Various 5-[[(acetamidophen-4-yl)oxy]methyl]-2-(p-substituted phenylamino)-1,3,4-oxadiazoles (4a-4d) were synthesized by cyclization of the corresponding N1-[[(acetamidophen-4-yl)oxy]acetyl]- N4-(p-substituted phenylamino)-3-thiosemicarbazides (3a-3d). All four of the thiosemicarbazides [250 mg/kg, orally (p.o.)] and the corresponding oxadiazoles (250 ...
L V, Nargund, G R, Reddy, V, Hariprasad
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THE CHEMISTRY OF 1,3,4-OXADIAZOLE DERIVATIVES
Russian Chemical Reviews, 1964CONTENTS I. Introduction 508 II. Preparation of mono-substituted 1,3,4-oxadiazoles 508 III. Preparation of symmetrical 2,5-substituted 1,3,4-oxadiazoles 508 IV. Preparation of asymmetrical 2,5-substituted 1,3,4-oxadiazoles 509 V. Preparation of poly-1,3,4-oxadiazoles 511 VI.
E P Nesynov, A P Grekov
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ChemInform, 2014
AbstractCompound (IIIb) is found to exhibit slightly higher antioxidant activity than the standard ascorbic acid.
Guda Mallikarjuna Reddy +5 more
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AbstractCompound (IIIb) is found to exhibit slightly higher antioxidant activity than the standard ascorbic acid.
Guda Mallikarjuna Reddy +5 more
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