Laboratory of steroid compounds

2020

Iodine-Promoted Synthesis of Pyrazoles from 1,3-Dicarbonyl Compounds and Oxamic Acid Thiohydrazides
Anna Komendantova, Konstantine Lyssenko, Igor Zavarzin and Yulia Volkova
Org. Chem. Front. 2020, 7, 1640-1646. https://doi.org/10.1039/D0QO00476F

Development of 1,3-thiazole Analogues of Imidazopyridines as Potent Positive Allosteric Modulators of GABA receptors
Tatyana Tikhonova, Irina Rassokhina, Eugene Kondrakhin, Mikhail Fedosov, Julia Bukanova, Alexey Rossokhin, Irina Sharonova, Georgy Kovalev, Igor Zavarzin and Yulia Volkova
Bioorg. Chem. 2020, 94, 103334. https://doi.org/10.1016/j.bioorg.2019.103334

Sulfur-Mediated Synthesis of Unsymmetrically Substituted N-aryl Oxalamides by the Cascade Thioamidation/Cyclocondensation and Hydrolysis Reaction
Tatyana Tikhonova, Nikita Ilment, Konstantine Lyssenko, Igor Zavarzin and Yulia Volkova
Org. Biomol. Chem. 2020, 18, 5050-5060. https://doi.org/10.1039/D0OB00811G

Fe(III)-Catalyzed Synthesis of Steroidal Imidazoheterocycles as Potent Antiproliferative Agents

Anastasia Ilina, Yulia Volkova, Igor Zavarzin, Alexander Scherbakov, Diana Salnikova, Yaroslav Dzichenka, Valerii Shirinian, et al.
Org. Biomol. Chem. 2020, 18, 5571-5576. https://doi.org/10.1039/D0OB01241F

Novel D-annulated Pentacyclic Steroids: Regioselective Synthesis and Biological Evaluation in Breast Cancer Cells
Svetlana Vorontsova, Anton Yadykov, Alexander Scherbakov, Igor Zavarzin, Ekaterina Mikhaevich, Yulia Volkova and Valerii Shirinian
Molecules, 2020, 25 (15), 3499. https://doi.org/10.3390/molecules25153499

Regioselective Baeyer-Villiger Oxidation of Steroidal Ketones Into Lactones by BF3/H2O2 system
Alexey Ilovaisky, Valentina Merkulova, Vera Vil, Elena Chernoburova, Marina Shchetinina, Sergey Loguzov, Andrey Dmitrenok, Igor Zavarzin, Alexander Terent’ev
Eur. J. Org. Chem. 2020, 3, 402-405. https://doi.org/10.1002/ejoc.201901701

A Convenient Synthesis of New (1,2,4-pyrazolylamino)pyrimidines From Cyanamide Precursor
Mikhail Prezent, Sergey Baranin and Yuri Bubnov
Mendeleev Commun. 2020, 30, 4, 500-501. https://doi.org/10.1016/j.mencom.2020.07.032

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