M. Tarasenko

发表

Room-temperature synthesis of pharmaceutically important carboxylic acids bearing the 1,2,4-oxadiazole moiety

A. V. Smirnov, S. Baykov, A. Shetnev, 2017 .

Entry into (E)-3-(1,2,4-oxadiazol-5-yl)acrylic acids via a one-pot ring-opening/ring-closing/retro-Diels-Alder reaction sequence

V. Boyarskiy, S. Baykov, S. Presnukhina, 2020 .

2-(1,2,4-Oxadiazol-5-yl)anilines Based on Amidoximes and Isatoic Anhydrides: Synthesis and Structure Features

S. Baykov, A. Shetnev, M. Tarasenko, 2021, Russian Journal of General Chemistry.

2‐(1,2,4‐Oxadiazol‐5‐yl)aniline as a New Scaffold for Blue Luminescent Materials

V. Boyarskiy, I. Boyarskaya, S. Baykov, 2022, ChemistrySelect.

Selective reduction of 5-alkenyl-3-(nitrophenyl)-1,2,4-oxadiazoles to 5-alkenyl-3-(aminophenyl)-1,2,4-oxadiazoles

M. Tarasenko, E. R. Kofanov, S. Baikov, 2017, Russian Journal of Organic Chemistry.

Unusual Formation of 1,2,4-Oxadiazine Core in Reaction of Amidoximes with Maleic or Fumaric Esters

V. Boyarskiy, S. Baykov, S. Presnukhina, 2022, Molecules.

Synthesis and Study of the Structure of Palladium(II) Acyclic Diaminocarbene Complexes Containing a 1,2,4-Oxadiazole Moiety

M. Tarasenko, S. Baikov, M. A. Kinzhalov, 2020, Russian Journal of General Chemistry.

Application of amidoximes for the heterocycles synthesis

V. Boyarskiy, S. Baykov, M. Tarasenko, 2020 .

Synthesis and Photoluminescent Properties of 2-(3-Carboxymethylindazol-1-yl)anilines

S. Baykov, A. Shetnev, M. Tarasenko, 2021, Russian Journal of General Chemistry.

One-pot synthesis of 3,5-disubstituted 1,2,4-oxadiazoles containing an alkenyl moiety

M. Tarasenko, V. Sidneva, Evgeniy R. Kofanov, 2022, Chemistry of Heterocyclic Compounds.

Synthesis and Evaluation of Antibacterial Activity of 1,2,4-Oxadiazole-Containing Biphenylcarboxylic Acids

S. Presnukhina, A. Shetnev, M. Tarasenko, 2020, Russian Journal of General Chemistry.

π–π Noncovalent Interaction Involving 1,2,4- and 1,3,4-Oxadiazole Systems: The Combined Experimental, Theoretical, and Database Study

V. Boyarskiy, A. Novikov, M. Gureev, 2021, Molecules.

Diastereoselective Opening of Bridged Anhydrides by Amidoximes Providing Access to 1,2,4-Oxadiazole/Norborna(e)ne Hybrids

S. Baykov, A. Shetnev, M. Tarasenko, 2019, European Journal of Organic Chemistry.

External oxidant-free and transition metal-free synthesis of 5-amino-1,2,4-thiadiazoles as promising antibacterials against ESKAPE pathogen strains

V. Sharoyko, S. Baykov, A. Shetnev, 2022, Molecular Diversity.

One-Pot Synthesis of 3,5-Disubstituted 1,2,4-Oxadiazoles Using Catalytic System NaOH‒DMSO

M. Tarasenko, T. Sharonova, E. R. Kofanov, 2018, Russian Journal of Organic Chemistry.

Dualism of 1,2,4-Oxadiazole Ring in Noncovalent Interactions with Carboxylic Group

V. Boyarskiy, S. Baykov, A. Shetnev, 2022, Journal of Molecular Structure.

Synthesis and Biological Activity of 3-Aryl-5-(aryloxymethyl)-1,2,4-oxadiazoles

E. Vasilieva, S. Presnukhina, A. Shetnev, 2022, Russian Journal of Organic Chemistry.

Synthesis of 3,5-Disubstituted-1,2,4-oxadiazole Sulfonamides in the Superbasic t-BuONa/DMAA System

A. Shetnev, M. Tarasenko, J. A. Efimova, 2022, Russian journal of general chemistry.

Convenient entry to N-pyridinylureas with pharmaceutically privileged oxadiazole substituents via the acid-catalyzed C H activation of N-oxides

V. Boyarskiy, S. Baykov, Vladislava V. Matveevskaya, 2019, Tetrahedron Letters.

1,2,4-Oxadiazole/2-Imidazoline Hybrids: Multi-target-directed Compounds for the Treatment of Infectious Diseases and Cancer

V. Sharoyko, A. Rozhkov, S. Kalinin, 2019, International journal of molecular sciences.

An efficient synthesis and antimicrobial evaluation of 5-alkenyl- and 5-styryl-1,2,4-oxadiazoles

M. Kuznetsov, S. Baykov, A. Shetnev, 2018, ARKIVOC.

Metal-free hydroarylation of the side chain carbon–carbon double bond of 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles in triflic acid

A. Ivanov, I. Boyarskaya, A. Vasilyev, 2017, Beilstein journal of organic chemistry.