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ACS Combinatorial Science|February 1, 2014
Toward lead-oriented synthesis: one-pot version of Castagnoli condensation with nonactivated alicyclic anhydridesSergey V Ryabukhin, Dmitriy M Panov, Dmitry S Granat, et al.
The Journal of Organic Chemistry|May 20, 2024
Toward a Chemical Constructor: A Lego-Like Approach for Formal α-Alkylation of Cyclic KetonesAndriy I Frolov, Yaroslav O Chuchvera, Eugeniy N Ostapchuk, et al.
The Journal of Organic Chemistry|January 13, 2026
Expanding the Synthetic Scope of Rawal's Diene: Access to Pyran and Pyrazole DerivativesOleksii I Shamrai, Eugeniy N Ostapchuk, Dmytro O Leha, et al.
The Journal of Organic Chemistry|May 27, 2021
Selective α-Methylation of KetonesAndriy I Frolov, Eugeniy N Ostapchuk, Alexander E Pashenko, et al.
Organic Letters|September 14, 2007
A one-step fusion of 1,3-thiazine and pyrimidine cyclesSergey V Ryabukhin, Andrey S Plaskon, Eugeniy N Ostapchuk, et al.
The Journal of Organic Chemistry|September 12, 2019
Far Away from Flatland. Synthesis and Molecular Structure of Dihetera[3.3.n]propellanes and Trihetera[3.3.n]propellanes: Advanced Analogues of Morpholine/PiperazineYevhenii M Sokolenko, Yevhen Yu Yurov, Bohdan V Vashchenko, et al.
The Journal of Organic Chemistry|December 10, 2024
Multigram Synthesis of 3,3-Spiro-α-prolinesNikita O Derkach, Kostiantyn V Levchenko, Ievgenii A Iermolenko, et al.
ACS Omega|August 29, 2019
Scalable Synthesis of Biologically Relevant Spirocyclic PyrrolidinesKostiantyn P Melnykov, Artem N Artemenko, Bohdan O Ivanenko, et al.
Organic & Biomolecular Chemistry|March 21, 2025
Concise practical avenues toward 5,5-spiro-α-prolinesIevgenii A Iermolenko, Artem A Artemenko, Dmytro O Vasko, et al.
Molecules (Basel, Switzerland)|February 11, 2023
Screening of Palladium/Charcoal Catalysts for Hydrogenation of Diene Carboxylates with Isolated-Rings (Hetero)aliphatic ScaffoldVladyslav V Subotin, Bohdan V Vashchenko, Vitalii M Asaula, et al.
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