Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Alexander Kazantsev"'
Publikováno v:
Molbank, Vol 2024, Iss 1, p M1768 (2024)
Carbazole polymers attract significant attention as promising luminophores, organic electronic and photovoltaic materials, photo/electrocatalysts, energy storage materials, redox mediators and catalysts. However, the oxidation potential of the commer
Externí odkaz:
https://doaj.org/article/1c1ee7ae4b054a5d924d0cc91bb1b3a3
Autor:
Mikhail Krasavin, Andrey Bubyrev, Alexander Kazantsev, Christopher Heim, Samuel Maiwald, Daniil Zhukovsky, Dmitry Dar’in, Marcus D. Hartmann, Alexander Bunev
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 37, Iss 1, Pp 527-530 (2022)
The advent of proteolysis-targeting chimaeras (PROTACs) mandates that new ligands for the recruitment of E3 ligases are discovered. The traditional immunomodulatory drugs (IMiDs) such as thalidomide and its analogues (all based on the phthalimide glu
Externí odkaz:
https://doaj.org/article/05018ca618a34ca08fb973d138964a14
Publikováno v:
Molecules, Vol 28, Iss 10, p 4209 (2023)
The use of spirocycles in drug discovery and medicinal chemistry has been booming in the last two decades. This has clearly translated into the landscape of approved drugs. Among two dozen clinically used medicines containing a spirocycle, 50% have b
Externí odkaz:
https://doaj.org/article/f263e5842ecc4b8ea16388e0cf560eec
Autor:
Alexei Lukin, Kristina Komarova, Lyubov Vinogradova, Marine Dogonadze, Tatiana Vinogradova, Piotr Yablonsky, Alexander Kazantsev, Mikhail Krasavin
Publikováno v:
Molecules, Vol 28, Iss 6, p 2529 (2023)
A small set of twelve compounds of a nitrofuran carboxamide chemotype was elaborated from a readily available 2,6-diazaspiro[3.4]octane building block, exploring diverse variants of the molecular periphery, including various azole substituents. The i
Externí odkaz:
https://doaj.org/article/2cec8e2e75fc42a3a5df91ef3fd42983
Publikováno v:
Molecules, Vol 27, Iss 23, p 8462 (2022)
Novel aryl-substituted homophthalic acids were cyclodehydrated to the respective homophthalic anhydrides for use in the Castagnoli–Cushman reaction. With a range of imines, this reaction proceeded smoothly and delivered hitherto undescribed 4-aryl-
Externí odkaz:
https://doaj.org/article/2ff071a96edf41a6ad1cc8dd949195e1
Autor:
Yannis Markonis, Mijael Rodrigo Vargas Godoy, Johanna Blöcher, Riya Dutta, Shailendra Pratap, Rajani Pradhan, Alexander Kazantsev, Petr Bašta, Akbar Rahmati, Arnau Sanz i Gil, Vishal Thakur, Hossein Abbasizadeh, Oldřich Rakovec, Martin Hanel, Petr Máca, Rohini Kumar, Simon Papalexiou
ITHACA is a 5-year project that aims to benchmark the terrestrial water cycle intensification. Our goal is to estimate the past range of the hydrological cycle variability, determine the present state of its acceleration, and understand its future im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2eddc0e86a70549dc5290fa8cb14dfa
https://doi.org/10.5194/egusphere-egu23-12775
https://doi.org/10.5194/egusphere-egu23-12775
Autor:
Mikhail Krasavin, Alexander Kazantsev
Publikováno v:
Expert Opinion on Therapeutic Patents. 32:171-190
Introduction Cereblon (CRBN), the substrate receptor of the CRL4CRBN E3 ubiquitin ligase has been extensively studied due to its involvement in many biological processes. It has also been identified as the target for immunomodulatory drugs (IMiDs). C
Publikováno v:
2022 International Ural Conference on Electrical Power Engineering (UralCon).
Autor:
Alexander Kazantsev, Olga Bakulina, Dmitry Dar’in, Grigory Kantin, Alexander Bunev, Mikhail Krasavin
Publikováno v:
Organic letters. 24(26)
An attempted Regitz diazo transfer onto homophthalic anhydride led to the discovery of an unexpected ring contraction, which gave
Autor:
Alexander Kazantsev, Ivan A. Rodionov, Olga Bakulina, Grigory Kantin, Dmitry Dar’in, Mikhail Krasavin
Publikováno v:
Catalysts
Volume 13
Issue 2
Pages: 428
Volume 13
Issue 2
Pages: 428
(E)-3-Arylidene-4-diazopyrrolidine-2,5-diones previously shown to yield two products in reactions with tetrahydrofuran mediated by rhodium carbenes—tetrahydrofur-2-yl-substituted product of C-H insertion and spirocyclic product of formal C-O insert