Zobrazeno 1 - 10
of 156
pro vyhledávání: '"Dmitry A. Loginov"'
Publikováno v:
Catalysts, Vol 13, Iss 2, p 389 (2023)
This work demonstrates the influence of the catalyst and alkyne nature on the regioselectivity of rhodium-catalyzed annulation of alkoxy-substituted benzoic acids (such as 3-methoxybenzoic, 3,4-dimethoxybenzoic, and piperonylic acids) with alkynes. H
Externí odkaz:
https://doaj.org/article/433122c5848340428642dcac40f8a428
Publikováno v:
Inorganics, Vol 10, Iss 10, p 158 (2022)
It has been shown that the interaction of tris(triphenylphosphine)ruthenium dichloride RuCl2(PPh3)3 (1) with 10-vertex monocarborane [6-Ph-nido-6-CB9H11]−[Et4N]+ (2) under mild thermolysis conditions is not selective due to the undesired coordinati
Externí odkaz:
https://doaj.org/article/c116f33f0ced4452bb87655bd9a0b643
Autor:
Pavel S. Gribanov, Dmitry A. Loginov, Dmitry A. Lypenko, Artem V. Dmitriev, Sergey I. Pozin, Alexey E. Aleksandrov, Alexey R. Tameev, Igor L. Martynov, Andrey Yu. Chernyadyev, Sergey N. Osipov
Publikováno v:
Molecules, Vol 26, Iss 24, p 7596 (2021)
Three new benzothiadiazole (BTD)-containing luminophores with different configurations of aryl linkers have been prepared via Pd-catalyzed cross-coupling Suzuki and Buchwald–Hartwig reactions. Photophysical and electroluminescent properties of the
Externí odkaz:
https://doaj.org/article/f241251cc3374b60b82ffc75513262a0
Autor:
Vladimir B. Kharitonov, Dmitry V. Muratov, Yulia V. Nelyubina, Ilya A. Shutkov, Alexey A. Nazarov, Dmitry A. Loginov
Publikováno v:
The Journal of Organic Chemistry. 88:2869-2883
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24784ea27e42979134e46aca1283fc25
https://doi.org/10.1021/acs.joc.2c02526
https://doi.org/10.1021/acs.joc.2c02526
Autor:
Alexander L. Rusanov, Daniil D. Romashin, Peter M. Kozhin, Maxim N. Karagyaur, Dmitry S. Loginov, Olga V. Tikhonova, Victor G. Zgoda, Nataliya G. Luzgina
Publikováno v:
Data, Vol 7, Iss 3, p 27 (2022)
The immortalized keratinocytes, HaCaT, are a popular model for skin research (toxicity, irritation, allergic reactions, or interaction of cells). They maintain a stable keratinocyte phenotype and respond to keratinocyte differentiation stimuli. Howev
Externí odkaz:
https://doaj.org/article/9296a820af3a4a74a06209fb7189aa2e
Autor:
Juan Luis Pacheco‐García, Ernesto Anoz‐Carbonell, Dmitry S. Loginov, Daniel Kavan, Eduardo Salido, Petr Man, Milagros Medina, Angel L. Pey
Publikováno v:
The FEBS Journal. 290:1855-1873
Our knowledge on the genetic diversity of the human genome is exponentially growing. However, our capacity to establish genotype–phenotype correlations on a large scale requires a combination of detailed experimental and computational work. This is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d638a4b58fc2169d169400fb0a0b54
https://doi.org/10.1111/febs.16677
https://doi.org/10.1111/febs.16677
Publikováno v:
Synthesis. 54:5119-5127
An efficient protocol has been developed for the synthesis of larger condensed arenes from aromatic hydrocarbons and internal alkynes. This protocol uses readily available [CpRhI2]n as a catalyst and Cu(OAc)2 as an oxidant and proceeds smoothly throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2efba255b5095a0cd681c14b6ba1adfb
https://doi.org/10.1055/s-0041-1737342
https://doi.org/10.1055/s-0041-1737342
Autor:
Klim Olegovich Biriukov, Oleg Ilyich Afanasyev, Maria Igorevna Godovikova, Dmitry Alexandrovich Loginov, Denis Alexandrovich Chusov
Publikováno v:
Russian Chemical Reviews. 91:1-34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43a9edbb15b6513546fd6a18c52ddee7
https://doi.org/10.1070/rcr5045
https://doi.org/10.1070/rcr5045
Autor:
Mikhail A. Arsenov, Nadezhda V. Stoletova, Tat'yana F. Savel'yeva, Alexander F. Smol'yakov, Victor I. Maleev, Dmitry A. Loginov, Vladimir A. Larionov
Publikováno v:
Organic & Biomolecular Chemistry. 20:9385-9391
The first asymmetric route to artificial amino acids with an isoquinolone skeleton was elaborated via a straightforward Rh(iii)-catalyzed C–H activation/annulation reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fcf8028be955b05868823e655721453
https://doi.org/10.1039/d2ob01970a
https://doi.org/10.1039/d2ob01970a
Publikováno v:
Russian Chemical Bulletin. 70:1922-1926
Rhodacarborane [(9-NMe3-7,8-C2B9H10)RhCl2]2 exhibited moderate catalytic activity in the reaction of annulation of arylcarboxylic acids with alkynes, giving naphthalenes as the major products. Effects of the substituent at the carborane ligand, as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34587dbacda92d87cac9afd58c0b23e2
https://doi.org/10.1007/s11172-021-3297-x
https://doi.org/10.1007/s11172-021-3297-x