Results 61 to 70 of about 3,169 (181)
Two novel extended electron‐deficient central cores (Tz‐Qx, Dz‐Qx) with F/Cl‐substituted terminal groups synergistically optimize small molecule acceptors. Tz‐Qx‐4F outperforms Dz‐Qx‐based counterparts, achieving 19.50% PCE (29.3 mA cm−2 JSC) when blended with D18, thus providing valuable insights for designing high‐performance organic solar cell ...
Lan Xie +10 more
wiley +1 more source
Synthesis of Oxadiazole Derivatives from Terephthalic Acid
Oxadiazoles, nitrogen-containing heterocycles, are attracting interest due to their promising biological activities. This study focuses on the synthesis of oxadiazole derivatives from functionalized intermediates derived from terephthalic acid, a ...
Fekih Yasmine +2 more
doaj +1 more source
Functionalized nitrile oxides have attracted increasing attention because the incorporated functional groups not only influence cycloaddition reactivity but also provide valuable handles for subsequent molecular diversification.
Nagatoshi Nishiwaki
doaj +1 more source
A series of 5-substituted-4-amino-1,2,4-triazole-3-thioesters was synthesized by converting variously substituted organic acids successively into the corresponding esters, hydrazides, 5-substituted-1,3,4-oxadiazole-2-thiols, 5-substituted-1,2,4-triazole ...
Aurangzeb Hasan +2 more
doaj +1 more source
We demonstrate modular modifications of the widely employed emitter 2,4,5,6‐tetra(9H‐carbazol‐9‐yl)isophthalonitrile (4CzIPN) by replacing one or both nitrile acceptors with oxadiazole groups via a tetrazole intermediate.
Fabian Hundemer +7 more
doaj +1 more source
An unparalleled copper(I)-catalyzed synthesis of 1,3,4-oxadiazoles from tertiary amines in one step has been described. The one-pot reactions involving (N-isocyanimine)triphenylphosphorane, tertiary amines, and carboxylic acids resulted in the formation ...
Mei Sun +10 more
doaj +1 more source
AbstractTuberculosis remains a leading global health threat, exacerbated by the emergence of multi‐drug‐resistant strains. The search for novel therapeutic agents is critical in addressing this challenge. This review systematically summarizes the potential of oxadiazole derivatives as promising candidates in antimycobacterial drug discovery.
openaire +2 more sources
Synthesis and Antibacterial Evaluation of 5-Aminosalicylic Acid Derivatives
The anti-inflammatory scaffold 5-aminosalicylic acid, which is widely used in therapeutic applications, was chosen for the synthesis of N-[3-(hydrazinecarbonyl)-4-hydroxyphenyl]acetamide (1) to enhance its antibacterial properties.
Kazimieras Anusevičius +6 more
doaj +1 more source
Glycogen phosporylase (GP) is a promising target for the control of glycaemia. The design of inhibitors binding at the catalytic site has been accomplished through various families of glucose-based derivatives such as oxadiazoles.
Marion Donnier-Maréchal +6 more
doaj +1 more source
Toxicological Evaluation of Anti-Scrapie Trimethoxychalcones and Oxadiazoles
An altered form of the cellular prion protein, the PrPScor PrPRes, is implicated in the occurrence of the still untreatable transmissible spongiform encephalopathies.
CLAUDIA P. FIGUEIREDO +10 more
doaj +1 more source

