Synthesis and antiproliferative studies of 5-aryl-2-(3-thienylamino)-1,3,4- thiadiazoles
A series of 5-aryl-2-(3-thienylamino)-1,3,4-thiadiazoles 3a-m were synthesized in good yields in two steps starting from thiophen-3- isothiocyanates.
Gadais, Charlène +4 more
core +1 more source
The palladium-catalyzed cross-coupling reactions of 3-chloro-4-halogeno-1,2,5-thiadiazoles
3,4-Dichloro- and 3-chloro-4-halogeno-1,2,5-thiadiazoles (halogeno-: bromo- and iodo-) are involved in Pd-catalyzed cross-coupling reactions under Stille and Suzuki conditions.
Alain Merschaert +3 more
core +1 more source
Design, Synthesis, and Biological Evaluation of Amide Derivatives of Coumarin-1,2,4-Thiadiazoles as Anticancer Agents. [PDF]
Lingala AK +3 more
europepmc +1 more source
Development of a Late-Stage Functionalization Strategy to Access Diverse 3,5-Disubstituted 1,2,4-Thiadiazoles. [PDF]
Dobria A +3 more
europepmc +1 more source
Recent Advances in the Synthesis and Applications of 1,2,3/1,2,5-Thiadiazole- and Benzo[<i>c</i>][1,2,5/1,2,3]thiadiazole-Type Compounds. [PDF]
Quiroga D, Rodríguez D, Coy-Barrera E.
europepmc +1 more source
An Imidazo[2,1-b][1,3,4]thiadiazole Derivative Inhibits the Virulence Factor α-Hemolysin by Blocking the Pullout of Its Stem Domain. [PDF]
Korotkov VS +9 more
europepmc +1 more source
Synthesis and characterization of FeCuAlO<sub>4</sub> as a reusable heterogeneous acidic nanocatalyst for preparation of 2-amino-1,3,4-thiadiazole derivatives in water. [PDF]
Nikoo A.
europepmc +1 more source
Design, Synthesis, and Investigation of the Biological Activities of New Thiadiazole Derivatives With Anticancer Effects. [PDF]
Özkay Y +5 more
europepmc +1 more source
Synthesis and biological screening of some halogenated thiadiazoles and triazoles
89-95 Acid hydrazide 1 is treated with aryl isothiocyanates to get corresponding thiosemicarbazides 2. Compounds 2 in acidic medium give thiadiazoles 3 and in basic medium give triazoles 4. These compounds are synthesized by conventional method and ultra
Saji, George +3 more
core
Utility of 3-(2-oxo-2H-chromen-3-yl)-1-phenyl-1H-pyrazole-4-carbaldehyde in the synthesis of novel 1,3,4-thiadiazoles or 1,3-thiazoles and study their cytotoxic activity. [PDF]
Abdel-Aziem A, Abdelhamid AO.
europepmc +1 more source

