Reaction of esters of PIII acids with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone


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Resumo

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.

Sobre autores

M. Gazizov

Kazan National Research Technological University

Autor responsável pela correspondência
Email: mukattisg@mail.ru
Rússia, 68 ul. K. Marksa, Kazan, 420015

R. Ismagilov

Kazan National Research Technological University

Email: mukattisg@mail.ru
Rússia, 68 ul. K. Marksa, Kazan, 420015

L. Shamsutdinova

Kazan National Research Technological University

Email: mukattisg@mail.ru
Rússia, 68 ul. K. Marksa, Kazan, 420015

A. Tarakanova

Kazan National Research Technological University

Email: mukattisg@mail.ru
Rússia, 68 ul. K. Marksa, Kazan, 420015

R. Karimova

Kazan National Research Technological University

Email: mukattisg@mail.ru
Rússia, 68 ul. K. Marksa, Kazan, 420015

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