Аннотация:
The one-step synthesis of a macrocyclic node was performed by the interaction of thiacalix[4]arene with ethylene chlorophosphite; new cyclic derivatives of calix[n]arenes containing phosphorus fragments at the lower rim in the 1,2- (n=4) and 1,2,3-alternate (n=6) configurations were obtained.
Образец цитирования:
I. I. Stoikov, O. A. Mostovaya, A. A. Yantemirova, I. S. Antipin, A. I. Konovalov, “Phosphorylation of p-tert-butyl(thia)calixarenes by ethylene chlorophosphite”, Mendeleev Commun., 22:1 (2012), 21–22
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2723
https://www.mathnet.ru/rus/mendc/v22/i1/p21
Эта публикация цитируется в следующих 10 статьяx:
A. A. Vavilova, I. E. Shiabiev, P. L. Padnya, I. I. Stoikov, ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference, 2390, ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference, 2022, 020084
Alena Vavilova, Pavel Padnya, Timur Mukhametzyanov, Aleksey Buzyurov, Konstantin Usachev, Daut Islamov, Marat Ziganshin, Artur Boldyrev, Ivan Stoikov, “2D Monomolecular Nanosheets Based on Thiacalixarene Derivatives: Synthesis, Solid State Self-Assembly and Crystal Polymorphism”, Nanomaterials, 10:12 (2020), 2505
A. I. Konovalov, I. S. Antipin, V. A. Burilov, T. I. Madzhidov, A. R. Kurbangalieva, A. V. Nemtarev, S. E. Solovieva, I. I. Stoikov, V. A. Mamedov, L. Ya. Zakharova, E. L. Gavrilova, O. G. Sinyashin, I. A. Balova, A. V. Vasilyev, I. G. Zenkevich, M. Yu. Krasavin, M. A. Kuznetsov, A. P. Molchanov, M. S. Novikov, V. A. Nikolaev, L. L. Rodina, A. F. Khlebnikov, I. P. Beletskaya, S. Z. Vatsadze, S. P. Gromov, N. V. Zyk, A. T. Lebedev, D. A. Lemenovskii, V. S. Petrosyan, V. G. Nenaidenko, V. V. Negrebetskii, Yu. I. Baukov, T. A. Shmigol', A. A. Korlyukov, A. S. Tikhomirov, A. E. Shchekotikhin, V. F. Traven', L. G. Voskresenskii, F. I. Zubkov, O. A. Golubchikov, A. S. Semeikin, D. B. Berezin, P. A. Stuzhin, V. D. Filimonov, E. A. Krasnokutskaya, A. Yu. Fedorov, A. V. Nyuchev, V. Yu. Orlov, R. S. Begunov, A. I. Rusakov, A. V. Kolobov, E. R. Kofanov, O. V. Fedotova, A. Yu. Egorova, V. N. Charushin, O. N. Chupakhin, Yu. N. Klimochkin, V. A. Osyanin, A. N. Reznikov, A. S. Fisyuk, G. , “Modern Trends of Organic Chemistry in Russian Universities”, Russ J Org Chem, 54:2 (2018), 157
A. A. Nazarova, L. I. Makhmutova, I. I. Stoikov, “Synthesis of pillar[5]arenes with a PH-containing fragment”, Russ J Gen Chem, 87:9 (2017), 1941
A. A. Vavilova, R. V. Nosov, I. I. Stoikov, “Selective fluoride ion recognition by a thiacalix[4]arene receptor containing N-(4-nitrophenyl)acetamide and 1-amidoanthraquinone fragments”, Mendeleev Commun., 26:6 (2016), 508–510
Fumio Hamada, Kunda Uma Maheswara Rao, Takashi Kimuro, Manabu Yamada, Yoshihiko Kondo, “Synthesis, X-Ray Structure and Metal Extracton Abilities of New Diethyl Phosphate Modified Thiacalix[4]arene”, HETEROCYCLES, 91:5 (2015), 989
Olga A. Mostovaya, Maria N. Agafonova, Andrey V. Galukhin, Bulat I. Khayrutdinov, Daut Islamov, Olga N. Kataeva, Igor S. Antipin, Alexander I. Konovalov, Ivan I. Stoikov, “Phosphorylated amino derivatives of thiacalix[4]arene as membrane carriers: synthesis and host–guest molecular recognition of amino, hydroxy and dicarboxylic acids”, J of Physical Organic Chem, 27:1 (2014), 57
Rajesh Kumar, Yeon Ok Lee, Vandana Bhalla, Manoj Kumar, Jong Seung Kim, “Recent developments of thiacalixarene based molecular motifs”, Chem. Soc. Rev., 43:13 (2014), 4824
V. A. Burilov, R. I. Nugmanov, R. R. Ibragimova, S. E. Solovieva, I. S. Antipin, A. I. Konovalov, “Microwave-assisted Alkylation of p-tert-butylcalix[4]arene Lower Rim: The Effect of Alkyl Halides”, Mendeleev Commun., 23:2 (2013), 113–115
И. Р. Князева, А. Р. Бурилов, М. А. Пудовик, В. Д. Хабихер, “Фосфорсодержащие макроциклические соединения: синтез и свойства”, Усп. хим., 82:2 (2013), 150–186; I. R. Knyazeva, A. R. Burilov, M. A. Pudovik, W. D. Habicher, “Phosphorus-containing macrocyclic compounds: synthesis and properties”, Russian Chem. Reviews, 82:2 (2013), 150–186