С. В. Курбатов

ORCID: 0000-0002-8886-5222
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Chemical Reaction Mechanisms
  • Synthesis and Biological Evaluation
  • Organic Chemistry Cycloaddition Reactions
  • Genetic Neurodegenerative Diseases
  • Synthesis and Characterization of Heterocyclic Compounds
  • Chemical Reactions and Mechanisms
  • Structural and Chemical Analysis of Organic and Inorganic Compounds
  • Mitochondrial Function and Pathology
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Synthesis and biological activity
  • Berberine and alkaloids research
  • Crystallography and molecular interactions
  • Synthesis and Reactions of Organic Compounds
  • Synthesis of heterocyclic compounds
  • Asymmetric Synthesis and Catalysis
  • Neurological diseases and metabolism
  • Muscle Physiology and Disorders
  • Hereditary Neurological Disorders
  • Synthesis and Characterization of Pyrroles
  • Synthesis and Reactivity of Heterocycles
  • Organic and Inorganic Chemical Reactions
  • Fluorine in Organic Chemistry
  • Ion channel regulation and function

Voronezh State Medical Academy named after N.N. Burdenko
2021-2025

Saratov State Medical University
2024-2025

Southern Federal University
2015-2024

Institute of Physics and Technology
2024

Yaroslavl State University
2018-2021

Voronezh Regional Clinical Oncology Center
2014-2020

Promundo
2018

Consultative and Diagnostic Center
2012-2017

Counseling Center
2015

Institut Lavoisier de Versailles
2003-2013

Valery N. Charushin Egor V. Verbitskiy О. Н. Чупахин Daria V. Vorobyeva Pavel S. Gribanov and 81 more Sergey N. Osipov А. В. Иванов Svetlana V. Martynovskaya Elena F. Sagitova V. D. Dyachenko I. V. Dyachenko S. G. Krivokolylsko В. В. Доценко А. В. Аксенов Дмитрий А. Аксенов Nicolai A. Aksenov Alexander А. Larin Леонид Л. Ферштат Vasiliy M. Muzalevskiy Valentine G. Nenajdenko Anna V. Gulevskaya А. Ф. Пожарский Ekaterina A. Filatova Kseniya V. Belyaeva Б.А. Трофимов Ирина А. Балова Natalia A. Danilkina Anastasia I. Govdi Alexander S. Tikhomirov Andrey E. Shchekotikhin Михаил С. Новиков Николай В. Ростовский Alexander F. Khlebnikov Yu. N. Klimochkin М. В. Леонова I. M. Tkachenko В. А. Мамедов Vera L. Mamedova Н. А. Жукова Vyacheslav E. Semenov Оleg G. Sinyashin Oleg V. Borshchev Yuriy N. Luponosov Sergey A. Ponomarenko Alexander S. Fisyuk Anastasia S. Kostyuchenko Vladimir G. Ilkin Tetyana Beryozkina Vasiliy А. Bakulev Almir S. Gazizov Almaz A. Zagidullin Andrey A. Karasik Maxim E. Kukushkin Елена К. Белоглазкина Никита Е. Голанцов Alexey А. Festa L. G. Voskresenskii Владимир С. Мошкин Evgeny M. Buev Vyacheslav Ya. Sosnovskikh Irina A. Mironova Павел С. Постников Viktor V. Zhdankin Mekhman S. Yusubov Ivan A. Yaremenko Vera A. Vil’ Igor B. Krylov Alexander O. Terent’ev Yulia G. Gorbunova Alexander G. Martynov А. Yu. Tsivadze Pavel A. Stuzhin Svetlana S. Ivanova O. I. Koifman Олег Н. Буров Михаил Е. Клецкий С. В. Курбатов Оlga I. Yarovaya Константин П. Волчо Нариман Ф. Салахутдинов M. A. Panova Yanina V. Burgart В. И. Салоутин Alsu R. Sitdikova Ekaterina S. Shchegravina Alexey Yu. Fedorov

The chemistry of heterocyclic compounds has traditionally been and remains a bright area chemical science in Russia. This is due to the fact that many heterocycles find widest application. These are key structural fragments most drugs, plant protection agents. Many natural also derivatives heterocycles. At present, more than half hundreds millions known collective review devoted achievements Russian chemists this field over last 15–20 years. presents leading heterocyclists representing both...

10.59761/rcr5125 article EN Russian Chemical Reviews 2024-07-01
А. И. Коновалов И. С. Антипин В. А. Бурилов Timur Madzhidov Almira R. Kurbangalieva and 74 more Andrey V. Nemtarev S. Е. Solovieva Ivan I. Stoikov В. А. Мамедов L. Ya. Zakharova Е. Л. Гаврилова Оleg G. Sinyashin Ирина А. Балова Aleksander V. Vasilyev И. Г. Зенкевич Mikhail Krasavin Михаил А. Кузнецов A. P. Molchanov Михаил С. Новиков Valerij A. Nikolaev L. L. Rodina Alexander F. Khlebnikov I. P. Beletskaya Sergey Z. Vatsadze С. П. Громов N. V. Zyk Аlbert T. Lebedev D. A. Lemenovśkii Valery S. Petrosyan В. Г. Ненайденко V. V. NEGREBETSKII YU. I. BAUKOV Tatiana A. Shmigol Аlexander А. Korlyukov Alexander S. Tikhomirov Andrey E. Shchekotikhin V. F. Traven Леонид Г. Воскресенский Федор И. Зубков О. А. Голубчиков А. С. Семейкин Д. Б. Березин Pavel A. Stuzhin В. Д. Филимонов E. A. Krasnokutskaya Alexey Yu. Fedorov Alexander V. Nyuchev V. Yu. Orlov Р. С. Бегунов А. И. Русаков A. V. Kolobov Е. Р. Кофанов О. В. Федотова A. Yu. Egorova Valery N. Charushin О. Н. Чупахин Yu. N. Klimochkin V. A. Osyanin A. N. Reznikov Alexander S. Fisyuk Г. П. Сагитуллина А. В. Аксенов Nicolai A. Aksenov М. К. Грачев Vera I. Maslennikova М. П. Коротеев A. K. BREL' С. В. Лисина С. М. Медведева Х. С. Шихалиев Г. А. Субоч М. С. Товбис Л. М. Миронович Sergey M. Ivanov С. В. Курбатов Михаил Е. Клецкий Олег Н. Буров К. И. Кобраков Д. Н. Кузнецов

10.1134/s107042801802001x article EN Russian Journal of Organic Chemistry 2018-02-01

Hereditary myopathy with early respiratory failure (HMERF) is caused by titin A-band mutations in exon 344 and considered quite rare. Respiratory insufficiency an symptom. A collection of families patients muscle disease suggestive HMERF was clinically genetically studied. Altogether 12 new 19 affected diverse nationalities were Most the investigated using targeted next-generation sequencing; Sanger sequencing applied some available family members. Histological data MRI findings evaluated....

10.1007/s00415-019-09187-2 article EN cc-by Journal of Neurology 2019-01-21

Leigh syndrome (LS), also known as infantile subacute necrotizing encephalopathy, is the most frequent mitochondrial disorder in children. Recently, more than 80 genes have been associated with LS, which greatly complicates diagnosis. In this article, we present clinical and molecular findings of 219 patients LS give detailed description three cases rare nuclear MORC2, NARS2 VPS13D, demonstrating wide genetic heterogeneity disease. The common cause Russian are pathogenic variants SURF1 gene...

10.3390/ijms24021597 article EN International Journal of Molecular Sciences 2023-01-13

LAMA2-associated muscular dystrophy is a rare genetic disorder caused by pathogenic or likely variants in the LAMA2 gene. The aim of this study to characterize spectrum pathogenic/likely gene among Russian patients, identify frequent specific population, and estimate prevalence Russia. Data were collected analyzed from patients with confirmed diagnoses using various molecular methods research centers 2008 2024. obtained 90 unrelated dystrophy, out which 83 presented more severe form, MDC1A1,...

10.3390/ijms26031257 article EN International Journal of Molecular Sciences 2025-01-31

ABSTRACT Spinal muscular atrophy 5q (5q SMA) is one of the most prevalent autosomal recessive disorders globally. The underlying cause SMA attributed to variants in SMN1 . Exon 7 not detectable major probands with SMA, and minor have a combination deletion an intragenic subtle variant second allele. From 1991 2023, DNA samples from 2796 representing unrelated families were analyzed at Research Centre for Medical Genetics diagnosis SMA. copy number SMN2 was determined all by MLPA....

10.1111/cge.14714 article EN Clinical Genetics 2025-02-04

Superelectrophilic 7-chloro-4,6-dinitrobenzofuroxan (DNBF-Cl) and 7-chloro-4,6-dinitrobenzofurazan (DNBZ-Cl) are shown to undergo facile carbon−carbon couplings with a series of weak carbon nucleophiles consisting number differently substituted indoles, 1,2,5-trimethylpyrrole azulene, in acetonitrile. Despite the fact that steric effects preclude coplanarity donor acceptor moieties, resulting substitution products subject an intense intramolecular charge transfer. A kinetic study various...

10.1021/jo900076r article EN The Journal of Organic Chemistry 2009-03-30

We developed a microfluidic synthesis with UV-Vis diagnostics using 3D printed chip for 8,13-disubstituted berberines. This system yielded up to 30% higher product yields high antioxidant activity compared traditional batch synthesis.

10.1039/d3nj04562e article EN New Journal of Chemistry 2023-12-05

Abstract The mechanism of the Diels–Alder interaction 4‐nitrobenzodifuroxan (NBDF) with cyclopentadiene (Cp), resulting in highly stereoselective formation stable endo [2+4] adduct has been elucidated by combining density functional theory (DFT) and experimental studies. Calculations at B3LYP/6‐31G* level reveal that this does not derive from a direct normal electron demand cycloaddition process. Instead, evidence is proceeds initially through very polar inverse process to afford...

10.1002/poc.1469 article EN Journal of Physical Organic Chemistry 2008-11-26

The kinetics of the coupling 4-nitrobenzodifuroxan (NBDF) with a series indoles 8 a-e to give expected Michael-type adducts 9 have been investigated in acetonitrile solution. No significant influence nature isotopic substitution at C-3 indole ring has found, indicating that NBDF addition step is rate limiting SEAr moiety. This implies measured second-order constants (k) for reactions are identical second order (k1NBDF) associated C--C step. By using known N and s parameters characterizing...

10.1002/chem.200700676 article EN Chemistry - A European Journal 2007-07-19

Nucleophilic aromatic substitutions (SNAr reactions) together with the formation of related σ-anionic adducts are reactions great importance in organic synthesis. 1 – 4 Scheme describes a ...

10.1080/00304948.2012.697701 article EN Organic Preparations and Procedures International 2012-01-01

Abstract The Diels–Alder reaction of 4‐nitrobenzodifuroxan (NBDF) with 1‐methoxy‐3‐trimethylsilyloxy‐1,3‐butadiene has been investigated experimentally and theoretically. Treatment NBDF excess diene in chloroform at room temperature was found to afford a single product that contained carbonyl functionality. Based on an X‐ray structure NMR spectroscopic data, the appeared be result hydrolysis OSiMe 3 moiety thermodynamically more stable endo [2+4] cycloadduct, characterized by cis arrangement...

10.1002/chem.201003695 article EN Chemistry - A European Journal 2011-05-17

Superelectrophilic halonitro-2,1,3-benzoxadiazoles under-go remarkably facile carbon–carbon couplings with some electron-rich aromatics and heteroaromatics, affording quantitatively products exhibiting an intense visible absorption due to strong intramolecular charge transfer.

10.1039/b307012c article EN Chemical Communications 2003-01-01

Coupling of superelectrophilic 4,6-dinitrobenzofuroxan with a π-excessive indolizine structure affords strongly dipolar substitution product which undergoes facile but unusual rearrangement induced by an intramolecular oxygen atom transfer from the N-oxide functionality DNBF moiety.

10.1039/b608350a article EN Chemical Communications 2006-01-01

A new approach for the annulation of a thiopyrane ring to an indole core under mild conditions was developed. Treating 2-methyl-3-acylindoles with lithium diisopropyl amide leads elimination proton from 2-methyl group. The indole-2,3-dienolates obtained were found react CS2 give corresponding thiopyrano[4,3-b]indole-3(5H)-thiones. mechanism represents stepwise addition through ion-pair formation, according PCM/B3LYP/6-311++G**, PBE1PBE/6-311++G**, and MP2//HF/6-311++G** quantum chemical...

10.1021/acs.joc.1c01200 article EN The Journal of Organic Chemistry 2021-08-02
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