888-71-1Relevant articles and documents
A Selective Synthesis of 3,5-Diphenyl-1,2,4-Oxadiazole by a Reaction of Benzylcobaloxime with Alkyl Nitrite
Kijima, Masashi,Nakazato, Katsuhiko,Sato, Takeo
, p. 347 - 348 (1994)
Benzyl ligand of Benzylbis(dimethylglyoximato)pyridine cobalt complexe was selectively converted to 3,5-diphenyl-1,2,4-oxadiazole by a reaction with alkyl nitrite under irradiation of visible light.The reaction proceeds via an in situ formation of an oxim
Synthesis method of 3, 5-disubstituted 1, 2, 4-oxadiazole
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Paragraph 0027-0030, (2021/06/22)
The invention relates to a novel synthetic method for synthesizing 3, 5-disubstituted-1, 2, 4-oxadiazole, in particular to a synthetic method of 3, 5-disubstituted-1, 2, 4-oxadiazole. The method disclosed by the invention has the characteristics that the reaction is carried out at room temperature, the 1, 2, 4-oxadiazole is synthesized at high yield by a one-pot method, and a final product does not need to be subjected to column chromatography. The 3, 5-disubstituted-1, 2, 4-oxadiazole synthesized by the invention can be used in the field of medical treatment.
Beyond direct Nrf2 activation; reinvestigating 1,2,4-oxadiazole scaffold as a master key unlocking the antioxidant cellular machinery for cancer therapy
Ayoup, Mohammed Salah,Abu-Serie, Marwa M.,Abdel-Hamid, Hamida,Teleb, Mohamed
, (2021/04/27)
Harnessing the antioxidant cellular machinery has sparked considerable interest as an efficient anticancer strategy. Activating Nrf2, the master switch of the cellular redox system, suppresses ROS, alleviates oxidative stress, and halts cancer progression