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Публикации


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Наиболее важные публикации

2026

Dyes and Pigments
Synthesis and photophysical properties of fluorophores based on enamino-substituted 4-methylene-1,4-dihydropyridines
A.E. Simbirtseva, I.V. Rozhina, D.L. Obydennov, M.Y. Kornev, V.Y. Sosnovskikh
к публикации

2025

Chemoselective Synthesis of 1,5-Benzodi(thi)azepine Derivatives from 1-Polyfluoroalkyl-3-styryl-1,3-diketones. Vladislav Y. Korotaev, Nikolay S. Zimnitskiy, Ivan A. Kochnev, Elizaveta M. Gomzikova, Anastasia D. Milchenko, Nikolay A. Tverdokhlebov, Oleg S. Eltsov, Alexey Y. Barkov, Vyacheslav Y. Sosnovskikh
ACS Omega
Chemoselective Synthesis of 1,5-Benzodi(thi)azepine Derivatives from 1-Polyfluoroalkyl-3-styryl-1,3-diketones
Vladislav Y. Korotaev, Nikolay S. Zimnitskiy, Ivan A. Kochnev, Elizaveta M. Gomzikova, Anastasia D. Milchenko, Nikolay A. Tverdokhlebov, Oleg S. Eltsov, Alexey Y. Barkov, Vyacheslav Y. Sosnovskikh
к публикации
De Novo Construction of Highly Substituted Chromones and Benzo[b]furans via a Switchable Transformation of 3-Alkynyl-4-pyrones with Active Methylene Compounds. Vladislav V. Fedin, Danil V. Syrovsky, Sergey A. Usachev, Dmitrii L. Obydennov, Vyacheslav Y. Sosnovskikh
Organic Letters
De Novo Construction of Highly Substituted Chromones and Benzo[b]furans via a Switchable Transformation of 3-Alkynyl-4-pyrones with Active Methylene Compounds
Vladislav V. Fedin, Danil V. Syrovsky, Sergey A. Usachev, Dmitrii L. Obydennov, Vyacheslav Y. Sosnovskikh
к публикации
Novel Solvent Promoted Synthesis of Furo[3,2‐c]pyridines from 3‐Alkynyl‐4‐pyrones: Synergy of a 4‐Pyrone and an α‐Alkynyl Enone Fragments. Vladislav V. Fedin, Sergey A. Usachev, Dmitrii L. Obydennov, Vyacheslav Y. Sosnovskikh
Asian Journal of Organic Chemistry
Novel Solvent Promoted Synthesis of Furo[3,2‐c]pyridines from 3‐Alkynyl‐4‐pyrones: Synergy of a 4‐Pyrone and an α‐Alkynyl Enone Fragments
Vladislav V. Fedin, Sergey A. Usachev, Dmitrii L. Obydennov, Vyacheslav Y. Sosnovskikh
к публикации
Halogen-Driven Chemospecific [3+2] Cycloaddition of Azomethine Ylides with Enals. Synthesis and Chemical Properties of 1-(Halovinyl)-2-Aminoethanols. Anastasia A. Smorodina, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
Asian Journal of Organic Chemistry
Halogen-Driven Chemospecific [3+2] Cycloaddition of Azomethine Ylides with Enals. Synthesis and Chemical Properties of 1-(Halovinyl)-2-Aminoethanols
Anastasia A. Smorodina, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации

Synthesis
Novel Synthesis of 3-Amino-2-pyrones and 3-Hydroxy-4-pyridones via Double Ring-Opening Reactions of 4-Pyrone Epoxides with Amines
Polina K. Titova, Nikita A. Alikin, Alexandrina V. Kaurova, Viktoria V. Viktorova, Alena E. Simbirtseva, Elena V. Steparuk, Oleg S. Eltsov, Dmitrii L. Obydennov, Vyacheslav Y. Sosnovskikh
к публикации
Molecular Diversity 
1-Styryl-1,3-diketones in the synthesis of spiro[oxindole-3,2′-pyrrolidines] with notable anticancer activity
Nikolay S. Zimnitskiy, Vladislav Y. Korotaev, Maria V. Ulitko, Vyacheslav Y. Sosnovskikh
к публикации
Organic Chemistry Frontiers
Three-step alkylaminomethylative α,β-difunctionalization of enones
Evgeny M. Buev, Vladimir S. Moshkin,Vyacheslav Y. Sosnovskikh
к публикации
The Team teachable
Tetrahedron Letters
3,4,5,6-Tetrahydro-2H-3,6-epoxybenzo[g][1,4]oxazocine – A new bridged heterocyclic system
Polina A. Khardina, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации
Organic & Biomolecular Chemistry
Regioselective synthesis of 5-azaindazoles based on the intramolecular amination reaction of 5-acyl-4-pyridones with hydrazines
Viktoria V. Viktorova, Dmitrii L. Obydennov, Alsu F. Mustafina, Maria V. Ulitko, Mikhail Y. Kornev and  Vyacheslav Y. Sosnovskikh
к публикации
Chemistry & Biodiversity 
The reaction of fenchone and camphor hydrazones with 5‐acyl‐4‐pyrones as a method for the synthesis of new polycarbonyl conjugates: tautomeric equilibrium and antiviral activity
Dmitrii L. Obydennov, Viktoria V. Viktorova, Kseniya S. Kovaleva, Olga I. Yarovaya, Shokhrukh A. Khasanov, Nikolay I. Bormotov, Iana L. Esaulkova, Olga A. Serova, Vladimir V. Zarubaev, Larisa N. Shishkina, Nariman F. Salakhutdinov, Vyacheslav Y. Sosnovskik
к публикации

2024

Synthesis of (2,3-dihydrobenzofuran-3-yl)acetic acids from salicylic aldehydes: Trimethylsilyl as traceless activating group
Tetrahedron Letters
Synthesis of (2,3-dihydrobenzofuran-3-yl)acetic acids from salicylic aldehydes: Trimethylsilyl as traceless activating group
Evgeny M. Buev, Polina A. Khardina, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации
Tetrahedron Letters
Diastereoselective synthesis of novel alkaloid-like 1,2,3,3a,7b,12-hexahydroindeno[2′,1′:2,3]indeno[1,2-c]pyrroles
Vladimir D. Fedorenko, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации

Russian Chemical Reviews
The chemistry of heterocycles in the 21st century (глава 2.21, стр. 217–227)
 Vladimir S. Moshkin, Evgeny M. Buev, Vyacheslav Y. Sosnovskikh
к публикации
Russian Journal of Organic Chemistry
Organic Chemistry in Russian Universities. Achievements of Recent Years, (глава 14).
Dmitrii L. Obydennov, Vyacheslav Y. Sosnovskikh
к публикации
Tetrahedron Letters
Novel synthesis of 2,3-dihydrobenzofuran-3-amines from salicylic aldehydes: Trimethylsilyl as traceless activating group
Polina A. Khardina, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации
The Journal of Organic Chemistry
Tunable Approach to Diverse Phenethylamines via Reduction of 5-Aryloxazolidines with Triethylsilane
Anastasia A. Smorodina, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации
The Journal of Organic Chemistry
Tunable Zinc-Mediated Reductive Cyclization of Diastereomeric 3-Nitro-4-phenacyl-2-(trihalomethyl)chromanes to Fused Pyrroline N-Oxides, Pyrrolines, and Pyrrolidines
Vladislav Y. Korotaev, Igor B. Kutyashev, Maxim S. Sannikov, Maria A. Mishchenko, Lyudmila S. Zavyalova, Ivan A. Kochnev, Alexey Y. Barkov, Nikolay S. Zimnitskiy, Vyacheslav Y. Sosnovskikh

к публикации
Tetrahedron Letters
Ring-opening of oxazolidines with acetone cyanohydrin: A short and effective pathway to 2-((2-hydroxyethyl)amino)acetonitriles from carbonyl compounds
Anastasia A. Smorodina, Evgeny M. Buev, Vladimir S. Moshkin, Vyacheslav Y. Sosnovskikh
к публикации
Люминофоры на основе 2,6-бис(аминовинил)-4-метилен-1,4-дигидропиридина и способ их получения: патент на изобретение
Обыденнов, Д. Л., Симбирцева, А. Е., Сосновских, В. Я.
к патенту
Метил-3-арил-3a-нитро-4-(трифторметил)-1,2,3,3a,4,9b-гексагидрохромено[3,4-c]пиррол-1-карбоксилаты, обладающие цитотоксической активностью в отношении к клеткам линии карциномы шейки матки человека HeLa, и способ их получения: патент на изобретение

Коротаев, В. Ю., Барков, А. Ю., Кочнев, И. А., Улитко, М. В., Зимницкий, Н. С., Сосновских, В. Я.

к патенту

2023

Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond
Tetrahedron Letters
Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond

Smorodina, A., Buev, E., Moshkin, V., Sosnovskikh, V.

к публикации
Synthesis of 3,6-substituted 2-methylthio-4-pyrones by acylation of ketene dithioacetals via soft enolization
Tetrahedron Letters
Synthesis of 3,6-substituted 2-methylthio-4-pyrones by acylation of ketene dithioacetals via soft enolization
Usachev, S. A., Fedin, V. V., Obydennov, D., Sosnovskikh, V. Y.
к публикации
The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones
Molecules
The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones
Viktorova, V. V., Steparuk, E. V., Obydennov, D. L., Sosnovskikh, V. Y.
к публикации
4-Hydroxy-2-pyrones: Synthesis, Natural Products, and Application
Organics
4-Hydroxy-2-pyrones: Synthesis, Natural Products, and Application
Fedin, V., Obydennov, D., Usachev, S., Sosnovskikh, V
к публикации
A novel strategy for the functionalization and design of 4-methylene-4H-pyran merocyanines via enamination and 1,8-conjugate addition
Organic & Biomolecular Chemistry
A novel strategy for the functionalization and design of 4-methylene-4H-pyran merocyanines via enamination and 1,8-conjugate addition
Obydennov, D. L., Simbirtseva, A. E., Shirinkin, A. S., Kornev, M. Y., Sosnovskikh, V. Y.
к публикации
Arylethanolamines in Ritter reaction: Synthesis of 2,4‐Diarylimidazole Core
Asian Journal of Organic Chemistry
Arylethanolamines in Ritter reaction: Synthesis of 2,4‐Diarylimidazole Core
Smorodina, A. A., Buev, E. M., Moshkin, V. S., Sosnovskikh, V. Y.
к публикации
Hemicurcuminoids (1-styryl-1,3-diketones) – valuable multi-faceted building blocks for organic synthesis
New Journal of Chemistry
Hemicurcuminoids (1-styryl-1,3-diketones) – valuable multi-faceted building blocks for organic synthesis
Zimnitskiy, N. S., Korotaev, V. Y., Barkov, A. Y., Kochnev, I. A., Sosnovskikh, V. Y.
к публикации
Oxidative Ring-Opening Transformation of 5-Acyl-4-pyrones as an Approach for the Tunable Synthesis of Hydroxylated Pyrones and Furans
The Journal of Organic Chemistry
Oxidative Ring-Opening Transformation of 5-Acyl-4-pyrones as an Approach for the Tunable Synthesis of Hydroxylated Pyrones and Furans
Steparuk, E., Meshcheryakova, E. A., Viktorova, V., Ulitko, M., Obydennov, D., Sosnovskikh, V
к публикации
Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones
Molbank
Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones
Steparuk, E. V., Obydennov, D. L., Sosnovskikh, V. Y.
к публикации

2022

Different Behavior of 2-Substituted 3-Nitro-2H-chromenes in the Reaction with Stabilized Azomethine Ylides Generated from α-Iminoesters
Molecules
Different Behavior of 2-Substituted 3-Nitro-2H-chromenes in the Reaction with Stabilized Azomethine Ylides Generated from α-Iminoesters
Kochnev, I. A., Barkov, A. Y., Simonov, N. S., Ulitko, M. V., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
2-(2-(Dimethylamino)vinyl)-4H-pyran-4-ones as Novel and Convenient Building-Blocks for the Synthesis of Conjugated 4-Pyrone Derivatives
Molecules
2-(2-(Dimethylamino)vinyl)-4H-pyran-4-ones as Novel and Convenient Building-Blocks for the Synthesis of Conjugated 4-Pyrone Derivatives
Obydennov, D. L., Nigamatova, D. I., Shirinkin, A. S., Melnikov, O. E., Fedin, V. V., Usachev, S. A., Simbirtseva, A. E., Kornev, M. Y., Sosnovskikh, V. Y.
к публикации
Straightforward synthesis of 3-substituted pyrrolidines from active methylene compounds, sarcosine and formaldehyde
Tetrahedron Letters
Straightforward synthesis of 3-substituted pyrrolidines from active methylene compounds, sarcosine and formaldehyde
Gorbunova, E. V., Moshkin, V. S., Fedorenko, V. D., Khardina, P. A., Buev, E. M., Sosnovskikh, V. Y.
к публикации
Green and Efficient Construction of Chromeno[3,4-c]pyrrole Core via Barton–Zard Reaction from 3-Nitro-2H-chromenes and Ethyl Isocyanoacetate
Molecules
Green and Efficient Construction of Chromeno[3,4-c]pyrrole Core via Barton–Zard Reaction from 3-Nitro-2H-chromenes and Ethyl Isocyanoacetate
Kochnev, I. A., Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
Phosphonium ylides in the multicomponent synthesis of pyrrolidines
Tetrahedron Letters
Phosphonium ylides in the multicomponent synthesis of pyrrolidines
Buev, E. M., Khardina, P. A., Moshkin, V. S., Sosnovskikh, V. Y.
к публикации
Russian Chemical Bulletin
Synthesis of 2,3-heterofused chromones, hetero analogues of xanthone
Sosnovskikh, V. Y.
к публикации
An AgOAc-catalyzed reaction of 3-nitro-2H-chromenes with ethyl diazoacetate: an efficient one-pot synthesis of ethyl 3,4-dihydrochromeno[3,4-c]pyrazole-1-carboxylates
Chemistry of Heterocyclic Compounds
An AgOAc-catalyzed reaction of 3-nitro-2H-chromenes with ethyl diazoacetate: an efficient one-pot synthesis of ethyl 3,4-dihydrochromeno[3,4-c]pyrazole-1-carboxylates
Bykova, L. S., Kochnev, I., Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
Molecules
Reactions of Trifluorotriacetic Acid Lactone and Hexafluorodehydroacetic Acid with Amines: Synthesis of Trifluoromethylated 4-Pyridones and Aminoenones
Fedin, V. V., Usachev, S. A., Obydennov, D. L., Sosnovskikh, V. Y.
к публикации
The synthesis and cytotoxic activity of N-unsubstituted 3-aryl-4-(trifluoromethyl)-4H-spiro[chromeno[3,4-c]pyrrolidine-1,11'-indeno[1,2-b]quinoxalines]
Chemistry of Heterocyclic Compounds
The synthesis and cytotoxic activity of N-unsubstituted 3-aryl-4-(trifluoromethyl)-4H-spiro[chromeno[3,4-c]pyrrolidine-1,11'-indeno[1,2-b]quinoxalines]
Barkovskii, S. V., Ulitko, M. V., Barkov, A. Y., Kochnev, I. А., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y., Stepanyuk, R. А., Madzhidov, T. I.
к публикации
Highly diastereoselective annulation of 2-substituted 3-nitro-2H-chromenes with hemicurcuminoids and curcuminoids via a double and triple Michael reaction cascade
New Journal of Chemistry
Highly diastereoselective annulation of 2-substituted 3-nitro-2H-chromenes with hemicurcuminoids and curcuminoids via a double and triple Michael reaction cascade
Zimnitskiy, N. S., Barkov, A. Y., Kochnev, I. A., Kutyashev, I. B., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
Research on Chemical Intermediates
Synthesis of 4-oxo-6-styryl-4H-pyran-2-carbonitriles and their application for the construction of new 4-pyrone derivatives
Obydennov, D. L., Simbirtseva, A. E., Sosnovskikh, V. Y.
к публикации

2021

[3+2] Annulation of 2-substituted 3-nitro-2H-chromenes with mercaptoacetaldehyde: stereoselective synthesis of tetrahydro-4H-thieno[3,2-c]chromen-3-ols
Chemistry of Heterocyclic Compounds
[3+2] Annulation of 2-substituted 3-nitro-2H-chromenes with mercaptoacetaldehyde: stereoselective synthesis of tetrahydro-4H-thieno[3,2-c]chromen-3-ols
Barkov, A. Y., Kochnev, I. A., Simonov, N. S., Kutyashev, I. B., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
5-Aryloxazolidines as Reagents for Double Alkylation of Arenes: A Novel Synthesis of 4-Aryltetrahydroisoquinolines
Journal of Organic Chemistry
5-Aryloxazolidines as Reagents for Double Alkylation of Arenes: A Novel Synthesis of 4-Aryltetrahydroisoquinolines
Buev, E. M., Smorodina, A. A., Moshkin, V. S., Sosnovskikh, V. Y.
к публикации
Synthesis and Reactivity of Electron-Deficient 3-Vinylchromones
Synopen
Synthesis and Reactivity of Electron-Deficient 3-Vinylchromones
Sosnovskikh, V. Y.
к публикации
Reactions of 4-Pyrones with Azomethine Ylides as a Chemo-selective Method for the Construction of Multisubstituted Pyrano[2,3-c] pyrrolidines
Synthesis
Reactions of 4-Pyrones with Azomethine Ylides as a Chemo-selective Method for the Construction of Multisubstituted Pyrano[2,3-c] pyrrolidines
Obydennov, D. L., Steben'kov, V. D., Obydennov, K. L., Usachev, S. A., Moshkin, V. S., Sosnovskikh, V. Y.
к публикации
2-Aryl-6-Polyfluoroalkyl-4-Pyrones as Promising RF-Building-Blocks: Synthesis and Application for Construction of Fluorinated Azaheterocycles
Molecules
2-Aryl-6-Polyfluoroalkyl-4-Pyrones as Promising RF-Building-Blocks: Synthesis and Application for Construction of Fluorinated Azaheterocycles
Usachev, S. A., Nigamatova, D. I., Mysik, D. K., Naumov, N. A., Obydennov, D. L., Sosnovskikh, V. Y.
к публикации
Acenaphthenequinone-Based Stabilized Azomethine Ylides in (3+2) Cycloaddition Reactions with 1,5-diarylpent-4-ene-1,3-diones
Chemistry of Heterocyclic Compounds
Acenaphthenequinone-Based Stabilized Azomethine Ylides in (3+2) Cycloaddition Reactions with 1,5-diarylpent-4-ene-1,3-diones
Zimnitskiy, N. S., Barkov, A. Y., Kutyashev, I. B., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
Regio- and Stereoselective 1,3-dipolar Cycloaddition of Azomethine Ylides Based on Isatins and (thia)proline to 3-nitro-2-(trifluoro(trichloro)methyl)-2H-chromenes: Synthesis and Cytotoxic Activity of 6-(trihalomethyl)-spiro[chromeno(thia)pyrrolizidine-11,3'-indolin]-2'-ones
Chemistry of Heterocyclic Compounds
Regio- and Stereoselective 1,3-dipolar Cycloaddition of Azomethine Ylides Based on Isatins and (thia)proline to 3-nitro-2-(trifluoro(trichloro)methyl)-2H-chromenes: Synthesis and Cytotoxic Activity of 6-(trihalomethyl)-spiro[chromeno(thia)pyrrolizidine-11,3'-indolin]-2'-ones
Kutyashev, I. B., Ulitko, M. V., Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
Two approaches toward the regio- and stereoselective synthesis of N-unsubstituted 3-aryl-4-(trifluoromethyl)-4H-spiro-[chromeno[3,4-c]pyrrolidine-1,3'-oxindoles]
Chemistry of Heterocyclic Compounds
Two approaches toward the regio- and stereoselective synthesis of N-unsubstituted 3-aryl-4-(trifluoromethyl)-4H-spiro-[chromeno[3,4-c]pyrrolidine-1,3'-oxindoles]
Korotaev, V. Y., Barkovskii, S. V., Kutyashev, I. B., Ulitko, M. V., Barkov, A. Y., Zimnitskiy, N. S., Kochnev, I., Sosnovskikh, V. Y.
к публикации
1,5-Diarylpent-4-ene-1,3-diones in the synthesis of spiro[(thia)pyrrolizidine-3,3'-oxindoles] and 1,3-diaryl-5-spiro[oxindole-3,3'-pyrrolizidin-2'-yl]-1H-pyrazoles
Chemistry of Heterocyclic Compounds
1,5-Diarylpent-4-ene-1,3-diones in the synthesis of spiro[(thia)pyrrolizidine-3,3'-oxindoles] and 1,3-diaryl-5-spiro[oxindole-3,3'-pyrrolizidin-2'-yl]-1H-pyrazoles
Korotaev, V. Y., Zimnitskiy, N. S., Denikaev, A. D., Barkov, A. Y., Kutyashev, I. B., Sosnovskikh, V. Y.
к публикации
Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo­addition Reaction
Synopen
Diversity-Oriented Synthesis of Novel Trihalomethyl-Containing Spirochromeno[3,4-a](thia)pyrrolizidines and Spirochromeno-[3,4-a]indolizidines by One-Pot, Three-Component [3+2]-Cyclo­addition Reaction
Kutyashev, I. B., Sannikov, M. S., Kochnev, I. A., Barkov, A. Y., Zimnitskiy, N. S., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
Russian Chemical Reviews
SYNTHESIS AND REACTIVITY OF 3-(1-ALKYNYL)CHROMONES
Sosnovskikh, V. Y.
к публикации

2020

2,6-Dicyano-4-pyrone as a Novel and Multifarious Building Block for the Synthesis of 2,6-Bis(hetaryl)-4-pyrones and 2,6-Bis(hetaryl)-4-pyridinols
ACS Omega
2,6-Dicyano-4-pyrone as a Novel and Multifarious Building Block for the Synthesis of 2,6-Bis(hetaryl)-4-pyrones and 2,6-Bis(hetaryl)-4-pyridinols
Obydennov, D. L., Simbirtseva, A. E., Piksin, S. E., Sosnovskikh, V. Y.
к публикации
An expedient synthesis of novel spiro[indenoquinoxaline-pyrrolizidine]-pyrazole conjugates with anticancer activity from 1,5-diarylpent-4-ene-1,3-diones through the 1,3-dipolar cycloaddition/cyclocondensation sequence
New Journal of Chemistry
An expedient synthesis of novel spiro[indenoquinoxaline-pyrrolizidine]-pyrazole conjugates with anticancer activity from 1,5-diarylpent-4-ene-1,3-diones through the 1,3-dipolar cycloaddition/cyclocondensation sequence
Zimnitskiy, N. S., Barkov, A. Y., Ulitko, M. V., Kutyashev, I. B., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
3-Nitro-2-phenyl-2-trifluoromethyl-2H-chromenes in reactions with azomethine ylides from isatins and (thia)proline: synthesis of spiro[chromeno(thia)pyrrolizidine-11,3'-oxindoles]
Chemistry of Heterocyclic Compounds
3-Nitro-2-phenyl-2-trifluoromethyl-2H-chromenes in reactions with azomethine ylides from isatins and (thia)proline: synthesis of spiro[chromeno(thia)pyrrolizidine-11,3'-oxindoles]
Kutyashev, I. B., Kochnev, I., Cherepkova, A., Zimnitskiy, N. S., Barkov, A. Y., Korotaev, V. Y., Sosnovskikh, V. Y.
к публикации
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