10570-69-1Relevant articles and documents
": A Jack of Trio "-robust one-pot metal free oxidative amination, azidation and peroxidation of phenols
Sarkar, Debayan,Ghosh, Manoj Kumar,Rout, Nilendri,Kuila, Puspendu
supporting information, p. 3715 - 3718 (2017/07/12)
Herein we disclose a highly efficient methodology for the generation of nitrogen containing quaternary carbon centres via aminative and azidative oxidative dearomatization of phenols. The same protocol has also been successfully employed to achieve oxidative peroxidation of phenols. The simplest metal free reaction conditions delineate an easy breakthrough to the "Trio"- oxidative amination, azidation and peroxidation. An array of diverse polyfunctionalised heterocycles has been synthesized in one pot.
Migrations in Oxidations of Mesidine
Goldstein, Stephen L.,McNelis, Edward
, p. 1613 - 1620 (2007/10/02)
The oxidation of mesidine in methanolic media by ferricyanide, dichromate, and persulfate afforded an anil 4 containing a shifted methoxymethyl group in addition to the principal anil 3 formed by oxidative dealkylation.Possible intermediates 6, 7, and 8 were prepared and oxidized to the product anils.Oxidations of related anilines 9, 10, and 13 did not parallel those of mesidine but afforded analogues of 3.There is significant spectral evidence for anils with alkyl shifts but little for anils analogous to 4.
UNUSUAL DISPROPORTIONATION ENCOUNTERED IN THE ALUMINA-CATALYZED DEHYDRATION OF 4-(α-HYDROXYETHYL)PHENOLS
Kamogawa, Hiroyoshi,Watanabe, Motoshi,Oka, Saichiro,Nanasawa, Masato
, p. 793 - 794 (2007/10/02)
Alumina-catalyzed dehydrations of 4-(α-hydroxyethyl)phenols provided unusual disproportionation products: 4-ethylphenols and 4-acetylphenols and their tautomers.