Vitalii A. Krasilnikov
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Vitalii A. Krasilnikov has a total of 18 co-authors. Here are the top co-authors by number of shared publications:
- Nataliya Pavlovna Belskaya
Department of Technology for Organic Synthesis, Ural Federal University, 19 Mira Str., Yekaterinburg 620012, Russia
4 shared publications - Artyom S Minin
Department of Technology for Organic Synthesis, Ural Federal University, 19 Mira Str., Yekaterinburg, 620002, Russia
2 shared publications - Enrico Benassi
Infochemistry Scientific Center, ITMO University, Saint-Petersburg 191002, Russian Federation
2 shared publications Timur O. Fomin
Department of Technology for Organic Synthesis, Ural Federal University, 19 Mira Str., Yekaterinburg, 620002, Russia
2 shared publications- Aleksandr Yu. Vakhrushev
Herzen State Pedagogical University of Russia
1 shared publication - Andrey S. Smirnov
Department of Organic Chemistry, Institute of Chemistry, St. Petersburg State University
1 shared publication
Latest Publications
- 29 January 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 14 (8) , 2530-2542
Photocleavable luminescent conjugates of 2-(2-aryl-5-(piperidin-1-yl)-2 H -1,2,3-triazol-4-yl)thiazoles and aminoacids, diagnostics and drugs
We developed highly fluorescent photocages based on a 2-aryl-1,2,3-thiazol-4-yl-1,2,3-thiazole core. Extensive experimental and theoretical studies demonstrated their excellent properties compared to published light-based masking systems.
- 29 January 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 14 (8) , 2530-2542
Photocleavable luminescent conjugates of 2-(2-aryl-5-(piperidin-1-yl)-2 H -1,2,3-triazol-4-yl)thiazoles and aminoacids, diagnostics and drugs
We developed highly fluorescent photocages based on a 2-aryl-1,2,3-thiazol-4-yl-1,2,3-thiazole core. Extensive experimental and theoretical studies demonstrated their excellent properties compared to published light-based masking systems.
- 17 November 2025
- Published by Royal Society of Chemistry (RSC) in CrystEngComm
- Vol. 27 (45) , 7390-7398
Divergent noncovalent interactions of isomeric nitrile and isocyanide groups in selenodiazole–triazole cocrystals: σ-hole chalcogen bonding versus π–π stacking
Functional nitrile and isocyanide groups form noncovalent bonds with different donor centers in the cocrystals of functionalized 1,2,3-triazole with selenodiazole.
- 17 November 2025
- Published by Royal Society of Chemistry (RSC) in CrystEngComm
- Vol. 27 (45) , 7390-7398
Divergent noncovalent interactions of isomeric nitrile and isocyanide groups in selenodiazole–triazole cocrystals: σ-hole chalcogen bonding versus π–π stacking
Functional nitrile and isocyanide groups form noncovalent bonds with different donor centers in the cocrystals of functionalized 1,2,3-triazole with selenodiazole.
- 27 February 2025
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 90 (10) , 3590-3602
Isothiazole Construction by Metal-Free Reactions of Thioamides with Iminoiodinanes and Their Photophysical Properties
Metal-free reactions of thioacetamide derivatives with N-sulfonyliminoiodinane, affording isothiazoles under mild conditions, are described. 2-Substituted thioacetamides modified with an enamine moiety undergo reactions with iminoiodinane to form 4,5-disubstituted isothiazoles in 72-93% yields. Reactions of (het)arylidene-substituted 2-thioacetamides and iminoiodinane with subsequent one-pot oxidation of the formed sulfonylisothiazolines afford 3,4,5-trisubstituted isothiazoles in 44-96% yields. A scale-up synthesis of the developed methods was performed. The photophysical properties of the new isothiazoles were investigated, and UV- or blue-light-shifted fluorescence has been detected (QY up to 11%).
- 27 February 2025
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 90 (10) , 3590-3602
Isothiazole Construction by Metal-Free Reactions of Thioamides with Iminoiodinanes and Their Photophysical Properties
Metal-free reactions of thioacetamide derivatives with N-sulfonyliminoiodinane, affording isothiazoles under mild conditions, are described. 2-Substituted thioacetamides modified with an enamine moiety undergo reactions with iminoiodinane to form 4,5-disubstituted isothiazoles in 72-93% yields. Reactions of (het)arylidene-substituted 2-thioacetamides and iminoiodinane with subsequent one-pot oxidation of the formed sulfonylisothiazolines afford 3,4,5-trisubstituted isothiazoles in 44-96% yields. A scale-up synthesis of the developed methods was performed. The photophysical properties of the new isothiazoles were investigated, and UV- or blue-light-shifted fluorescence has been detected (QY up to 11%).