The Kabachnik–Fields Reaction in the Synthesis of Polyaminophosphonate Derivatives of p-tert-Butylthiacalix[4]arene
- 作者: Shibaeva K.1, Mostovaya O.1, Nazarova A.1, Shurpik D.1, Shiabiev I.1, Kuznetsova D.1, Stoykov I.1
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隶属关系:
- Butlerov Chemistry Institute
- 期: 卷 88, 编号 9 (2018)
- 页面: 1812-1817
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222405
- DOI: https://doi.org/10.1134/S1070363218090086
- ID: 222405
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详细
Novel derivatives of p-tert-butylthiacalix[4]arene containing four or eight 1-aminophosphonate groups at the lower rim of the macrocycle in 1,3-alternate conformation have been synthesized via the Kabachnik–Fields reaction. These compounds are promising synthetic receptors for biologically important acids. It has been shown that complete phosphorylation of the first generation dendrimer containing eight primary amino groups is impeded in the case of cyclic ketones.
作者简介
K. Shibaeva
Butlerov Chemistry Institute
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
O. Mostovaya
Butlerov Chemistry Institute
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
A. Nazarova
Butlerov Chemistry Institute
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
D. Shurpik
Butlerov Chemistry Institute
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
I. Shiabiev
Butlerov Chemistry Institute
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
D. Kuznetsova
Butlerov Chemistry Institute
Email: ivan.stoikov@mail.ru
俄罗斯联邦, ul. Kremlevskaya 18, Kazan, Tatarstan, 420008
I. Stoykov
Butlerov Chemistry Institute
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