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
- 作者: Padnya P.1, Bayarashov Е.1, Potrekeeva О.1, Stoikov I.1
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隶属关系:
- Butlerov Institute of Chemistry
- 期: 卷 87, 编号 9 (2017)
- 页面: 2111-2114
- 栏目: 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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详细
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.
作者简介
P. Padnya
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
Е. Bayarashov
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
О. Potrekeeva
Butlerov Institute of Chemistry
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
I. Stoikov
Butlerov Institute of Chemistry
编辑信件的主要联系方式.
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
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