ãCu(II)-Catalyzed Ortho C(sp2)-H Diarylamination of Arylamines To Synthesize Triarylaminesã?was published in Organic Letters in 2020. These research results belong to Kumar, Mohit; Sharma, Rishabh; Raziullah; Khan, Afsar Ali; Ahmad, Ashfaq; Dutta, Himangsu Sekhar; Koley, Dipankar. Synthetic Route of C3H6O2 The article mentions the following:
A copper-catalyzed, directed ortho C-H diarylamination of indoles, indolines, anilines, and N-aryl-7-azaindoles has been established. Only copper salt as the catalyst and oxygen as the terminal oxidant are used to synthesize triarylamines using various diarylamines including carbazole and phenothiazine. Mechanistic interrogation reveals that copper plays a dual role. The results came from multiple reactions, including the reaction of Oxetan-3-ol(cas: 7748-36-9Synthetic Route of C3H6O2)
Oxetan-3-ol(cas: 7748-36-9) is used as a reagent in the synthesis of 5-fluoro-4,6-dialkoxypyrimidine GPR119 agonists. It is also used as a reagent in the synthesis of cyclic sulfone hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors.Synthetic Route of C3H6O2
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