Results 191 to 200 of about 37,093 (255)
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Novel 1,3,4-oxadiazoles as antitubercular agents with limited activity against drug-resistant tuberculosis.

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
semanticscholar   +1 more source

ChemInform Abstract: 1,3,4‐Oxadiazole

ChemInform, 2014
AbstractReview: 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
openaire   +1 more source

Recent Advancement in Synthesis and Bioactivities of 1,3,4-Oxadiazole

Current Organic Synthesis, 2023
Abstract: 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
openaire   +2 more sources

Novel syntheses of symmetrical 2,5-diaryl-1,3,4-oxadiazoles and 1,4-phenylenebis-1,3,4-oxadiazoles

Russian Chemical Bulletin, 1998
The 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
openaire   +1 more source

Perfluoro-bis-1,3,4 oxadiazoles

Bulletin of the Academy of Sciences, USSR Division of Chemical Science, 1965
1. 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
openaire   +1 more source

Mechanistic studies on tandem cascade [4 + 2]/ [3 + 2] cycloaddition of 1,3,4-oxadiazoles with olefins.

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
semanticscholar   +1 more source

Aliphatic poly‐1,3,4‐oxadiazoles

Journal of Polymer Science Part A: General Papers, 1965
AbstractThree 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
openaire   +1 more source

Anti-inflammatory Activity of Substituted 1,3,4-Oxadiazoles

Journal of Pharmaceutical Sciences, 1994
Various 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
openaire   +2 more sources

THE CHEMISTRY OF 1,3,4-OXADIAZOLE DERIVATIVES

Russian Chemical Reviews, 1964
CONTENTS 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
openaire   +1 more source

ChemInform Abstract: Synthesis and Antioxidant Activity of Styrylsulfonylmethyl 1,3,4‐Oxadiazoles, Pyrazolyl/Isoxazolyl‐1,3,4‐oxadiazoles.

ChemInform, 2014
AbstractCompound (IIIb) is found to exhibit slightly higher antioxidant activity than the standard ascorbic acid.
Guda Mallikarjuna Reddy   +5 more
openaire   +1 more source

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