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Scianowski Jacek
Scianowski Jacek
Zweryfikowany adres z chem.umk.pl
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An update on “Selenium containing compounds from poison to drug candidates: a review on the GPx-like activity”
AJ Pacuła, F Mangiavacchi, L Sancineto, JL Eder, J Ścianowski, C Santi
Current chemical biology 9 (2), 97-112, 2016
872016
New glutathione peroxidase mimetics—Insights into antioxidant and cytotoxic activity
AJ Pacuła, KB Kaczor, A Wojtowicz, J Antosiewicz, A Janecka, A Długosz, ...
Bioorganic & Medicinal Chemistry 25 (1), 126-131, 2017
562017
Highly efficient synthesis and antioxidant capacity of N-substituted benzisoselenazol-3 (2 H)-ones
AJ Pacuła, J Ścianowski, KB Aleksandrzak
RSC Advances 4 (90), 48959-48962, 2014
542014
Convenient route to dialkyl diselenides from alkyl tosylates. Synthesis of di (cis-myrtanyl) diselenide
J Ścianowski
Tetrahedron letters 46 (19), 3331-3334, 2005
542005
Syntheses and reactions of new optically active terpene dialkyl diselenides
J Ścianowski, Z Rafiński, A Wojtczak
European journal of organic chemistry 2006 (14), 3216-3225, 2006
492006
Selenium‐Catalyzed Oxacyclization of Alkenoic Acids and Alkenols
L Sancineto, F Mangiavacchi, C Tidei, L Bagnoli, F Marini, A Gioiello, ...
Asian Journal of Organic Chemistry 6 (8), 988-992, 2017
482017
New chiral ebselen analogues with antioxidant and cytotoxic potential
AJ Pacuła, KB Kaczor, J Antosiewicz, A Janecka, A Długosz, T Janecki, ...
Molecules 22 (3), 492, 2017
482017
Synthesis and reactions of enantiomerically pure dialkyl diselenides from the p-menthane group
Z Rafiński, J Ścianowski
Tetrahedron: Asymmetry 19 (10), 1237-1244, 2008
442008
Syntheses and reactions of terpene β-hydroxyselenides and β-hydroxydiselenides
J Ścianowski, Z Rafiński, A Wojtczak, K Burczyński
Tetrahedron: Asymmetry 20 (24), 2871-2879, 2009
392009
New chiral selenium electrophiles derived from functionalized terpenes
J Ścianowski, Z Rafiński, A Szuniewicz, A Wojtczak
Tetrahedron 65 (49), 10162-10174, 2009
382009
Asymmetric selenocyclization with the use of dialkyl monoterpene diselenides
Z Rafiński, J Ścianowski, A Wojtczak
Tetrahedron: Asymmetry 19 (2), 223-230, 2008
302008
The Use of Sulfides Derived from Carane, P-Menthane, Pinane, and Bornane in the Synthesis of Optically Active Epoxides
A Banach, J Ścianowski, P Ozimek
Phosphorus, Sulfur, and Silicon and the Related Elements 189 (2), 274-284, 2014
282014
Synthesis and reactions of the optically active selenols derived from monoterpenes
J Ścianowski, J Rafalski, A Banach, J Czaplewska, A Komoszyńska
Tetrahedron: Asymmetry 24 (18), 1089-1096, 2013
262013
Synthesis and reactions of the optically active dialkyl diselenides from the pinane group
Z Rafinski, J Scianowski, A Wojtczak
Letters in Organic Chemistry 6 (4), 321-328, 2009
242009
Bioselectivity induced by chirality of new terpenyl organoselenium compounds
M Obieziurska, AJ Pacuła, A Długosz-Pokorska, M Krzemiński, A Janecka, ...
Materials 12 (21), 3579, 2019
212019
Application of Organolithium and Related Reagents in Synthesis. Part 111. Metallation of 2-Methyl- and 4-Methylnicotinic Acids. A Useful Method for Preparation of …
J Epsztajn, MW Płotka, J Ścianowski
Synthetic communications 22 (9), 1239-1247, 1992
211992
Sodium Selenosulfate from Sodium Sulfite and Selenium Powder: An Odorless Selenylating Reagent for Alkyl Halides to Produce Dialkyl Diselenide Catalysts
Y Liu, H Ling, C Chen, Q Xu, L Yu, X Jiang
Synlett 30 (14), 1698-1702, 2019
192019
Application of organolithium and related reagents in synthesis, Part X. Metallation-electrophilic substitution sequence of secondary chlorobenzamides
J Epsztajn, A Bieniek, JA Kowalska, J Ścianowski
Monatshefte für Chemie/Chemical Monthly 123 (12), 1125-1134, 1992
191992
Synthesis of Novel C2-Symmetric Sulfur-Based Catalysts: Asymmetric Formation of Halo-and Seleno-Functionalized Normal-and Medium-Sized Rings
S Jana, A Verma, V Rathore, S Kumar
Synlett 30 (14), 1667-1672, 2019
182019
Electrophilic selenium reagents: Addition reactions to double bonds and selenocyclizations
J Ścianowski, Z Rafiński
Organoselenium Chemistry: Between Synthesis and Biochemistry, 8-60, 2014
182014
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