Effect of the alkylidene spacer and the p-tert-butylthiacalix[4]arene macrocyclic platform on the reactivity of the hydroxyl groups in the acylation reaction
- Авторы: Padnya P.1, Bayarashov Е.1, Potrekeeva О.1, Stoikov I.1
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Учреждения:
- Butlerov Institute of Chemistry
- Выпуск: Том 87, № 9 (2017)
- Страницы: 2111-2114
- Раздел: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/221305
- DOI: https://doi.org/10.1134/S107036321709033X
- ID: 221305
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Аннотация
A series of cone and 1,3-alternate p-tert-butylthiacalix[4]arenes tetrasubstituted at the lower rim simultaneously by the amide, ester, and carboxyl functions were synthesized. The reactivity of the synthesized compounds depends on the length of the alkylidene spacer. The N-(hydroxyethyl)amide derivatives do not react with succinic anhydride, whereas the N-(3-hydroxypropyl)amide derivatives react to form acylation products.
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Об авторах
P. Padnya
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
Россия, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
Е. Bayarashov
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
Россия, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
О. Potrekeeva
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
Россия, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
I. Stoikov
Butlerov Institute of Chemistry
Автор, ответственный за переписку.
Email: ivan.stoikov@mail.ru
Россия, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
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