Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Aleksandra M. Puzyk"'
Autor:
Ivan S. Ershov, Kirill A. Esikov, Olga M. Nesterova, Mariya A. Skryl’nikova, Andrey V. Khramchikhin, Nadezda T. Shmaneva, Ivan S. Chernov, Ekaterina N. Chernova, Aleksandra M. Puzyk, Eugene V. Sivtsov, Yuliya N. Pavlyukova, Rostislav E. Trifonov, Vladimir A. Ostrovskii
Publikováno v:
Molbank, Vol 2023, Iss 1, p M1598 (2023)
3-(5-Phenyl-2H-tetrazol-2-yl)pyridine was synthesized by treating 5-phenyl-1H-tetrazole with pyridin-3-ylboronic acid under Chan–Evans–Lam coupling conditions. The structure and identity were confirmed by 1H, 13C-NMR spectroscopy, IR spectroscopy
Externí odkaz:
https://doaj.org/article/0daa7f1d69ca48bdb6418d65c60a8357
Autor:
Daria M. Krygina, Eugene V. Sivtsov, Yuliya N. Pavlyukova, Ekaterina N. Chernova, Mariya A. Skryl’nikova, Vadim A. Baigildin, Aleksandra M. Puzyk, Alexander A. Oskorbyn, Rostislav E. Trifonov, Pavel A. Aleshunin, Vladimir A. Ostrovskii
Publikováno v:
Molbank, Vol 2023, Iss 1, p M1565 (2023)
Highly purified 5-vinyl-1H-tetrazole was synthesized, which is in great demand in modern medicine and industry as a monomer for obtaining nitrogen-rich macromolecular compounds and a reagent for the complete synthesis of biological compounds. The mol
Externí odkaz:
https://doaj.org/article/e6e652318e234b8ba17c6307a8299e1b
Autor:
Andrey V. Khramchikhin, Mariya A. Skryl’nikova, Iana L. Esaulkova, Ekaterina O. Sinegubova, Vladimir V. Zarubaev, Maxim A. Gureev, Aleksandra M. Puzyk, Vladimir A. Ostrovskii
Publikováno v:
Molecules, Vol 27, Iss 22, p 7940 (2022)
This study of the interaction system of binucleophilic 3-substituted 4-amino-4H-1,2,4-triazole-5-thiols and 3-phenyl-2-propynal made it possible to develop a new approach to synthesis of such isomeric classes as 7-benzylidene-[1,2,4]triazolo[3,4-b][1
Externí odkaz:
https://doaj.org/article/a8c1e5f826574dec9a1c2d9641285a24
Publikováno v:
The Journal of Organic Chemistry. 87:6459-6470
Autor:
Artyom A. Yakubenko, Aleksandra M. Puzyk, Vladislav O. Korostelev, Valeriia V. Mulloyarova, Elena Yu. Tupikina, Peter M. Tolstoy, Alexander S. Antonov
Publikováno v:
Physical Chemistry Chemical Physics. 24:7882-7892
Self-association of diphenylpnictoginic acids Ph2XOOH was studied in solution and solid state. Diphenylbismuthinic and diphenylantimonic acids form polymeric covalent adducts, while diphenylphosphinic and diphenylarsinic form H-bonded associates.
Autor:
Vladimir Y. Mikshiev, Peter M. Tolstoy, Elena Yu. Tupikina, Aleksandra M. Puzyk, Mikhail A. Vovk
Publikováno v:
New Journal of Chemistry. 46:16471-16484
Molecular design by means of quantum-chemistry to improve an acid catalysed acyl-migration reaction through protonated amide nitrogen atom in carboxamides.
Autor:
Andrey V, Khramchikhin, Mariya A, Skryl'nikova, Iana L, Esaulkova, Ekaterina O, Sinegubova, Vladimir V, Zarubaev, Maxim A, Gureev, Aleksandra M, Puzyk, Vladimir A, Ostrovskii
Publikováno v:
Molecules (Basel, Switzerland). 27(22)
This study of the interaction system of binucleophilic 3-substituted 4-amino-4
Publikováno v:
Journal of Computational Chemistry. 42:2014-2023
This work is devoted to investigations of the influence of O-H···Se(-) hydrogen bonds on the electronic shells of selenolate R-Se(-) fragment (R═CH3 ). The geometric, energetic and nuclear magnetic resonance (NMR) spectral parameters for various
Publikováno v:
Journal of computational chemistryREFERENCES. 42(28)
This work is devoted to investigations of the influence of O-H···Se(-) hydrogen bonds on the electronic shells of selenolate R-Se(-) fragment (R═CH
Publikováno v:
Lecture Notes in Earth System Sciences ISBN: 9783030216139
Solubility of hydroxyapatite in aqueous solutions and artificial blood serum was studied at 37 ℃. The obtained results demonstrate non-monotonous changes of the concentration of calcium ions in solution over time: the respective curves contain a ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b369b3734e5630db0ec34d7f274f50ca
https://doi.org/10.1007/978-3-030-21614-6_3
https://doi.org/10.1007/978-3-030-21614-6_3