Zobrazeno 1 - 10
of 108
pro vyhledávání: '"A. I. Govdi"'
Autor:
Anastasia I. Govdi, Polina V. Tokareva, Andrey M. Rumyantsev, Maxim S. Panov, Johannes Stellmacher, Ulrike Alexiev, Natalia A. Danilkina, Irina A. Balova
Publikováno v:
Molecules, Vol 27, Iss 10, p 3191 (2022)
Cu-catalyzed 1,3-dipolar cycloaddition of ethyl 2-azidoacetate to iodobuta-1,3-diynes and subsequent Sonogashira cross-coupling were used to synthesize a large series of new triazole-based push–pull chromophores: 4,5-bis(arylethynyl)-1H-1,2,3-triaz
Externí odkaz:
https://doaj.org/article/2339ba8db8a54f16b09a5bc87564a0ce
Autor:
Anastasia I. Govdi, Sergey O. Anisimov, Natalia A. Danilkina, Alexander S. Bunev, Irina A. Balova
Publikováno v:
Mendeleev Communications. 33:328-330
Autor:
Mariia M. Efremova, Anastasia I. Govdi, Valeria V. Frolova, Andrey M. Rumyantsev, Irina A. Balova
Publikováno v:
Molecules, Vol 26, Iss 9, p 2801 (2021)
Cu-catalyzed 1,3-dipolar cycloaddition of methyl 2-azidoacetate to iodobuta-1,3-diynes and subsequent Suzuki-Miyaura cross-coupling were used to synthesize new triazoles derivatives: 5-aryl-4-arylethynyl-1H-1,2,3-triazoles. Investigation of their opt
Externí odkaz:
https://doaj.org/article/af733d9250694572818dd715f0caa068
Autor:
Sergey F. Vasilevsky, Denis S. Baranov, Anastasia I. Govdi, Irina V. Sorokina, Tatyana G. Tolstikova, Genrikh A. Tolstikov, Igor V. Alabugin
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 145-157 (2014)
Externí odkaz:
https://doaj.org/article/95dd029790ba49d1b76f3f2880a5eacb
Autor:
A. O. Shpakov, A. A. Bakhtyukov, A. A. Perminova, A. I. Govdi, I. V. Romanova, T. V. Sokolova, I. Yu. Morina, V. N. Sorokoumov, Kira V. Derkach
Publikováno v:
Journal of Evolutionary Biochemistry and Physiology. 57:208-220
Human chorionic gonadotropin (hCG) and luteinizing hormone (LH) regulate testicular steroidogenesis by interacting with the orthosteric site located in the extracellular domain of the LH receptor (LHR). The use of hCG and LH in medicine is fraught wi
Autor:
Natalia A. Danilkina, Nina S. Bukhtiiarova, Anastasia I. Govdi, Anna A. Vasileva, Andrey M. Rumyantsev, Artemii A. Volkov, Nikita I. Sharaev, Alexey V. Povolotskiy, Irina A. Boyarskaya, Ilya V. Kornyakov, Polina V. Tokareva, Irina A. Balova
Publikováno v:
Molecules, Vol 24, Iss 13, p 2386 (2019)
An efficient approach towards the synthesis of 6-aryl-4-azidocinnolines was developed with the aim of exploring the photophysical properties of 6-aryl-4-azidocinnolines and their click reaction products with alkynes, 6-aryl-4-(1,2,3-1H-triazol-1-yl)c
Externí odkaz:
https://doaj.org/article/ccfdd5a630504692a301de48ba28772f
Publikováno v:
Synthesis. 52:1874-1896
Copper-catalyzed azide–alkyne cycloaddition is a useful tool for the synthesis of both 1,2,3-triazoles and 5-iodo-1H-1,2,3-triazoles starting from either terminal alkynes or iodoalkynes. 5-Iodotriazoles have been recognized as very useful building
Autor:
Anastasia I. Govdi, Mariia M. Efremova, Andrey M. Rumyantsev, Valeria V. Frolova, Irina A. Balova
Publikováno v:
Molecules
Volume 26
Issue 9
Molecules, Vol 26, Iss 2801, p 2801 (2021)
Volume 26
Issue 9
Molecules, Vol 26, Iss 2801, p 2801 (2021)
Cu-catalyzed 1,3-dipolar cycloaddition of methyl 2-azidoacetate to iodobuta-1,3-diynes and subsequent Suzuki-Miyaura cross-coupling were used to synthesize new triazoles derivatives: 5-aryl-4-arylethynyl-1H-1,2,3-triazoles. Investigation of their opt
Autor:
Ilya V. Kornyakov, Stefan Bräse, Alexander S. D’yachenko, Alexander F. Khlebnikov, Irina A. Balova, Anastasia I. Govdi, Natalia A. Danilkina
Publikováno v:
The Journal of organic chemistry. 85(14)
The applicability of an intramolecular Nicholas reaction for the preparation of 10-membered O- and N-enediynes fused to indole, 1,2,3-triazole, and isocoumarin was investigated. The general approach to acyclic enediyne precursors fused to heterocycle
Autor:
Anastasia I. Govdi, Andrey M. Rumyantsev, Stefan Bräse, E. V. Sambuk, Anna G. Lyapunova, Mikhail V. Chislov, Galina L. Starova, Natalia A. Danilkina, Irina A. Balova, Alexander F. Khlebnikov
Publikováno v:
The Journal of Organic Chemistry. 83:2788-2801
To find promising analogues of naturally occurring enediyne antibiotics with a sufficient reactivity in the Bergman cyclization and moderately stable under isolation and storage, a scale of relative enediynes reactivity was created on the basis of ca