I. Mikhura

发表

Fluorescent nucleosides with an elongated rigid linker: attaching perylene to a nucleobase via a one-pot desilylation/Sonogashira reaction

A. Ustinov, S. V. Kutyakov, V. Korshun, 2016 .

Synthesis of ω-(4-hydroxyphenyl)alkanecarboxylic acids

S. Eremin, I. Mikhura, J. Yakovleva, 2000 .

C-Methylated Analogs of Spermine and Spermidine: Synthesis and Biological Activity

S. Kochetkov, A. Khomutov, I. Mikhura, 2019, Russian Journal of Bioorganic Chemistry.

Synthesis of macroheterocycles — Analogs of dibenzo-crown compounds. 4. 15–18-Membered pyridine-containing crown compounds

I. Mikhura, A. Formanovskii, 1989 .

Synthesis of Macrocyclic Compounds

I. Mikhura, A. Formanovskii, 1999 .

Characteristics of the Synthesis of Substituted and Condensed 2-Methyl-1,3-diazoles

I. Mikhura, A. Formanovsky, I. Popova, 2005 .

Interaction of 2-arylethyltin derivatives with triarylmethyl salts

I. Mikhura, O. Reutov, E. Uglova, 1985 .

Stereochemistry and mechanism of β-elimination reactions in tetraalkylstannanes

I. Mikhura, O. Reutov, E. Uglova, 1983 .

Synthesis of aza-crown compounds by intramolecular cyclization of ω-amino acids

I. Mikhura, A. Formanovskii, 1992 .

Convenient syntheses of phosphinic analogues of γ-aminobutyric- and glutamic acids

S. Kochetkov, D. De Biase, A. Khomutov, 2016, Russian Journal of Bioorganic Chemistry.

Tris(2,6-dimethoxyphenyl)methyl carbenium ion as a charge derivatization agent for the analysis of primary amines by MALDI mass spectrometry

R. Borisov, A. Ustinov, V. Korshun, 2016, Journal of Analytical Chemistry.

Effect of Photodynamic Antibacterial Chemotherapy Combined with Antibiotics on Gram-Positive and Gram-Negative Bacteria

I. Mikhura, F. Nakonechny, M. Nisnevitch, 2018, Molecules.

2-Ethynylperylene and improved synthesis of 3-ethynylperylene

A. Ustinov, S. V. Kutyakov, V. Korshun, 2016 .

Synthesis of mono- and di-O-sulfates of spacer-armed lactose

N. Bovin, A. Tuzikov, T. Ovchinnikova, 2015, Russian Chemical Bulletin.

Compounds based on 5-(perylen-3-ylethynyl)uracil scaffold: High activity against tick-borne encephalitis virus and non-specific activity against enterovirus A.

D. Osolodkin, G. Westman, B. Rathi, 2019, European journal of medicinal chemistry.

Improved Large-scale Synthesis of 5-(Perylen-3-ylethynyl)-arabino-uridine (aUY11), the Broad-Spectrum Antiviral

A. Ustinov, S. V. Kutyakov, V. Korshun, 2017 .

Unforeseen Possibilities To Investigate the Regulation of Polyamine Metabolism Revealed by Novel C-Methylated Spermine Derivatives

L. Alhonen, S. Kochetkov, A. Chizhov, 2019, Journal of medicinal chemistry.

Use of a Metallation Reaction to Obtain Substituted 2-(5-Methyl-2-thiazolyl)ethanols

I. Mikhura, A. Formanovsky, I. Popova, 2005 .

UR-144 in products sold via the Internet: identification of related compounds and characterization of pyrolysis products.

I. Mikhura, P. Kavanagh, S. Savchuk, 2013, Drug testing and analysis.

Cellulose fibrous sorbents with conformationally flexible aminocarboxylic groups for preconcentration of metals

Y. Zolotov, I. Mikhura, G. Tsysin, 1991 .

Synthesis of macroheterocyclic analogs of dibenzocrown ethers. 5. 16- and 17-Membered oxaazacrown ethers

I. Mikhura, A. Formanovskii, 1990 .

The total large-scale synthesis of argiopine

I. Mikhura, A. Formanovsky, I. Popova, 2009, Russian Journal of Bioorganic Chemistry.

Synthesis of macroheterocycles — Analogs of dibenzo-crown compounds. 18-Membered dioxadiaza-crown compounds

I. Mikhura, P. Terent’ev, A. S. Murakhovskaya, 1988 .

One-Stage Monosubstitution in Cyclen - Two Novel Examples

I. Mikhura, A. Formanovsky, 1996 .

One-Stage Monosubstitution in Cyclen. Two Novel Examples.

I. Mikhura, A. Formanovsky, 2010 .

Selective inhibitors of plasmepsin II of Plasmodium falciparum on the basis of pepstatin

A. G. Mikhailova, L. Rumsh, I. Mikhura, 2008, Russian journal of bioorganic chemistry.

Synthesis of Steroid Tracers by an Oxime Ligation Method and Their Use in Fluorescent Polarisation Immunoassay

V. Korshun, I. Mikhura, I. Prokhorenko, 2024, Russian Journal of Bioorganic Chemistry.