Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Svetlana S. Rybakova"'
Autor:
Dmitry S. Kopchuk, Alexey P. Krinochkin, Мaria I. Valieva, Еkaterina S. Starnovskaya, Yaroslav K. Shtaitz, Svetlana S. Rybakova, Evgeny D. Ladin, Ekaterina A. Kudryashova, Elvira R. Sharafieva, Оleg N. Chupakhin
Publikováno v:
Chimica Techno Acta, Vol 9, Iss 2 (2022)
The composition of the reaction mixture after DTTA tert-butyl ester alkylation with 6'-halomethyl-5-phenyl-2,2'-bipyridines was studied. In addition to the target product, DTTA-appended 2,2’-bipyridine, the corresponding 6'-hydroxymethyl-substitute
Externí odkaz:
https://doaj.org/article/a3e276a0706a4a1db9b25c6dc3838417
Autor:
Alexey P. Krinochkin, Мaria I. Savchuk, Еkaterina S. Starnovskaya, Igor L. Nikonov, Artem V. Baklykov, Ekaterina A. Kudryashova, Svetlana S. Rybakova, Evgeny D. Ladin, Dmitry S. Kopchuk, Zhuo Wang, Oleg N. Chupakhin
Publikováno v:
Chimica Techno Acta, Vol 8, Iss 4 (2021)
A new co-polymer based on fragments of 2-(2-pyridyl)monoazatriphenylene and 2,5-bis (2-ethylhexyl)-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione was prepared by using the Sonogashira reaction. The photophysical properties of the polymer
Externí odkaz:
https://doaj.org/article/58cb0939faf24bcc8c9409935ab004fc
Autor:
Alexey P. Krinochkin, Olga S. Taniya, Maria I. Savchuk, Ekaterina S. Starnovskaya, Yaroslav K. Shtaitz, Svetlana S. Rybakova, Dmitry S. Kopchuk, Igor S. Kovalev, Grigory V. Zyryanov, Oleg N. Chupakhin
Publikováno v:
AIP Conference Proceedings.
Autor:
Eugeny B. Gorbunov, Dmitry S. Kopchuk, Ekaterina A. Kudryashova, Svetlana S. Rybakova, Grigory V. Zyryanov, Oleg N. Chupakhin, Ekaterina S. Starnovskaya, Yaroslav K. Shtaitz, Alexey P. Krinochkin, Maria I. Savchuk
Publikováno v:
MODERN SYNTHETIC METHODOLOGIES FOR CREATING DRUGS AND FUNCTIONAL MATERIALS (MOSM2020): PROCEEDINGS OF THE IV INTERNATIONAL CONFERENCE.
Autor:
Grigory V. Zyryanov, Oleg N. Chupakhin, Dmitry S. Kopchuk, Sougata Santra, Svetlana S. Rybakova, Matiur Rahman, Albert F. Khasanov, Igor S. Kovalev
Publikováno v:
AIP Conference Proceedings.
A “Green" solvent-economic synthetic approach towards 5,11,17,23,29,35,41,47-octa-tert-butyl- 49,50,51,52,53,54,55,56-octaoxycalix[8]arene has been developed.