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Svetlana Yu. Vostruhina

Observed names: S. Yu. Vostruhina, S. Yu. Vostrukhina, Vostruhina, S. Y.
Observed institution: Samara State Technical University
ORCID: 0000-0002-0577-6153
Observed ORCID: 0000-0002-0577-6153
OpenAlex ID: A5028644356
Reductive Heck cyclization of cage containing compounds: Convenient access to adamantyl-substituted indolines and spiro-homoadamantane-oxindole
2022 · Alexander N. Reznikov, Maria A. Ashatkina, et al. · Tetrahedron Letters · 10
Intramolecular reductive Heck reaction in the synthesis of 3,3-disubstituted isoindolin-1-ones
2023 · M. A. Ashatkina, A. N. Reznikov, et al. · Russian Chemical Bulletin · 5
Asymmetric Reductive Heck Cyclization of 3-(Adamantan-1-yl)-1-(2-bromophenyl)prop-2-en-1-one: Highly Enantioselective Synthesis of 3-(Adamantan-1-yl)indan-1-one
2025 · A. N. Reznikov, S. Yu. Vostrukhina, et al. · Russian Journal of Organic Chemistry · 2
Palladium-catalyzed cyclization of N-(2-iodophenyl)acrylamides and hydrophosphoryl compounds in the presence of (R,R)-DIOP and (S)-Monophos ligands
2024 · S. Yu. Vostruhina, A. N. Reznikov, et al. · Russian Chemical Bulletin · 2
Asymmetric Synthesis of Isoindolin-1-ones from Enamides via Pd-Catalyzed Intramolecular Reductive Heck Reaction
2025 · M. A. Ashatkina, D. I. Shamshina, et al. · Russian Journal of General Chemistry · 1
Enantioselective Reductive Heck Reaction of Adamantyl-substituted Enones
2026 · S. Yu. Vostruhina, V. P. Popkov, et al. · Russian Journal of Organic Chemistry
Reductive heck cyclization and functionalyzation of 5-bromohomoadamant-4-ene carboxamide derivatives: The route to homoadamantene annulated heterocycles
2024 · Alexander N. Reznikov, Svetlana Yu. Vostruhina, et al. · Tetrahedron Letters
CCDC 2212925: Experimental Crystal Structure Determination
2022 · Reznikov, A. N., Ashatkina, M. A., et al. · The Cambridge Structural Database
CCDC 2210940: Experimental Crystal Structure Determination
2022 · Reznikov, A. N., Ashatkina, M. A., et al. · The Cambridge Structural Database
Works count: 9
Citation count: 20
H-index: 2
I10-index: 1
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