Reaction of esters of PIII acids with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone
- Авторы: Gazizov M.B.1, Ismagilov R.K.1, Shamsutdinova L.P.1, Tarakanova A.L.1, Karimova R.F.1
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Учреждения:
- Kazan National Research Technological University
- Выпуск: Том 65, № 12 (2016)
- Страницы: 2943-2947
- Раздел: Full Articles
- URL: https://journal-vniispk.ru/1066-5285/article/view/239681
- DOI: https://doi.org/10.1007/s11172-016-1682-7
- ID: 239681
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Аннотация
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.
Об авторах
M. Gazizov
Kazan National Research Technological University
Автор, ответственный за переписку.
Email: mukattisg@mail.ru
Россия, 68 ul. K. Marksa, Kazan, 420015
R. Ismagilov
Kazan National Research Technological University
Email: mukattisg@mail.ru
Россия, 68 ul. K. Marksa, Kazan, 420015
L. Shamsutdinova
Kazan National Research Technological University
Email: mukattisg@mail.ru
Россия, 68 ul. K. Marksa, Kazan, 420015
A. Tarakanova
Kazan National Research Technological University
Email: mukattisg@mail.ru
Россия, 68 ul. K. Marksa, Kazan, 420015
R. Karimova
Kazan National Research Technological University
Email: mukattisg@mail.ru
Россия, 68 ul. K. Marksa, Kazan, 420015
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