Reaction of esters of PIII acids with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone
- Autores: Gazizov M.B.1, Ismagilov R.K.1, Shamsutdinova L.P.1, Tarakanova A.L.1, Karimova R.F.1
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Afiliações:
- Kazan National Research Technological University
- Edição: Volume 65, Nº 12 (2016)
- Páginas: 2943-2947
- Seção: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/239681
- DOI: https://doi.org/10.1007/s11172-016-1682-7
- ID: 239681
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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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