58186-36-0Relevant articles and documents
Reaction of esters of PIII acids with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone
Gazizov,Ismagilov,Shamsutdinova,Tarakanova,Karimova
, p. 2943 - 2947 (2017/06/05)
A reaction of PIII acid esters with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone leads to the formation of phosphorylated phosphorus ylides, 3,3’,5,5’-tetra-tert-butylstilbenequinone, and diphosphorylated sterically hindered phenols. The schemes for the formation of these products through the primary key intermediates of betaine and phosphorus ylide structures were suggested.
Synthesis of organophosphorus derivatives of 2,6-di-tert-butyl-4- methylphenol
Prishchenko, Andrey A.,Livantsov, Mikhail V.,Novikova, Olga P.,Livantsova, Ludmila I.,Milaeva, Elena R.
, p. 490 - 494 (2008/12/21)
Convenient procedures for the synthesis of 2,6-di-tert-butyl-4-methylphenol (ionol) mono-, di-, and triphosphorus derivatives, starting from the readily accessible 3,5-di-tert-butyl-4-hydroxybenzaldehyde, are proposed, and some properties of the obtained
Synthesis of phosphorus derivatives of 2,6-di-tert-butyl-4-methylphenol
Prishchenko,Livantsov,Novikova,Livantsova,Shpakovskii,Milaeva
, p. 1753 - 1756 (2008/02/08)
Convenient procedures for the synthesis of 2,6-di-tert-butyl-4-methylphenol (ionol) mono-, di-and triphosphorus derivatives, starting from the readily accessible 3,5-di-tert-butyl-4-hydroxybenzaldehyde, are proposed, and some properties of the obtained co