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Mekhman S Yusubov

Explore the profile of Mekhman S Yusubov including associated specialties, affiliations and a list of published articles. Areas
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Articles 46
Citations 199
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Recent Articles
1.
Machulkin A, Petrov S, Bodenko V, Larkina M, Plotnikov E, Yuldasheva F, et al.
ACS Pharmacol Transl Sci . 2024 May; 7(5):1457-1473. PMID: 38751647
Lu-labeled small-molecule prostate-specific membrane antigen (PSMA) targeted tracers are therapeutic agents for metastatic castration-resistant prostate cancer. Optimizing molecular design holds the potential to further enhance the pharmacokinetic properties of PSMA-targeted...
2.
Yoshimura A, Ngo K, Mironova I, Gardner Z, Rohde G, Ogura N, et al.
Org Lett . 2024 Feb; 26(9):1891-1895. PMID: 38408024
Pseudocyclic arylbenziodoxaboroles are unique aryne precursors under neutral aqueous conditions that selectively react with organic sulfides, forming the corresponding sulfonium salts. This reaction is compatible with various substituents (alkyl, halogen,...
3.
Huss C, Yoshimura A, Rohde G, Mironova I, Postnikov P, Yusubov M, et al.
ACS Omega . 2024 Jan; 9(2):2664-2673. PMID: 38250385
Various five-membered cyclic dibenzobromolium salts (dibenzo[,]bromol-5-ium chloride, nitrate, hydrogen sulfate, dihydrogen phosphate, trifluoroacetate, and tetrafluoroborate) were prepared by diazotization-cyclization of 2'-bromo-[1,1'-biphenyl]-2-amine in solution of appropriate acids. The chlorolium analogues (iodide,...
4.
Radzhabov A, Ledneva A, Soldatova N, Fedorova I, Ivanov D, Ivanov A, et al.
Int J Mol Sci . 2023 Oct; 24(19). PMID: 37834088
We designed 0D, 1D, and 2D supramolecular assemblies made of diaryliodonium salts (functioning as double σ-hole donors) and carboxylates (as σ-hole acceptors). The association was based on two charge-supported halogen...
5.
Hasnowo L, Larkina M, Plotnikov E, Bodenko V, Yuldasheva F, Stasyuk E, et al.
Int J Mol Sci . 2023 Aug; 24(15). PMID: 37569582
Prostate-specific membrane antigen (PSMA) has been identified as a target for the development of theranostic agents. In our current work, we describe the design and synthesis of novel N-[N-[(S)-1,3-dicarboxypropyl]carbamoyl]-(S)-L-lysine (DCL)...
6.
Radzhabov A, Soldatova N, Ivanov D, Yusubov M, Kukushkin V, Postnikov P
Org Biomol Chem . 2023 Aug; 21(33):6743-6749. PMID: 37552120
We developed an atom- and reaction mass efficient strategy for the preparation of diarylselenides using iodonium salts as reactants. The developed approach allows the obtaining of diarylselenides from the corresponding...
7.
Mironova I, Noskov D, Yoshimura A, Yusubov M, Zhdankin V
Molecules . 2023 Mar; 28(5). PMID: 36903382
Hypervalent iodine reagents are in high current demand due to their exceptional reactivity in oxidative transformations, as well as in diverse umpolung functionalization reactions. Cyclic hypervalent iodine compounds, known under...
8.
Podrezova E, Okhina A, Rogachev A, Baykov S, Kirschning A, Yusubov M, et al.
Org Biomol Chem . 2023 Feb; 21(9):1952-1957. PMID: 36757159
The arylation of azaheterocycles can be considered as one of the most important processes for the preparation of various biologically active compounds. In the present work, we describe a method...
9.
Petrov S, Yusubov M, Beloglazkina E, Nenajdenko V
Int J Mol Sci . 2022 Nov; 23(22). PMID: 36430267
This review demonstrates the progress in the synthesis of radioiodinated compounds over the past decade. The possibilities and limitations of radiopharmaceuticals with different iodine isotopes, as well as the synthesis...
10.
Mironova I, Nenajdenko V, Postnikov P, Saito A, Yusubov M, Yoshimura A
Molecules . 2022 Jun; 27(12). PMID: 35744982
The intramolecular oxidative cycloaddition reaction of alkyne- or alkene-tethered aldoximes was catalyzed efficiently by hypervalent iodine(III) species to afford the corresponding polycyclic isoxazole derivatives in up to a 94% yield....