Works by Strobykina, I.
Results: 53
Synthesis and antimicrobial and antifungal activity of derivatives of the diterpenoid isosteviol and the glycoside steviolbioside containing onium nitrogen atoms.
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- Pharmaceutical Chemistry Journal, 2011, v. 44, n. 11, p. 597, doi. 10.1007/s11094-011-0525-y
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- Article
Synthesis and anti-tuberculous activity of diesters based on isosteviol and dicarboxylic acids.
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- Pharmaceutical Chemistry Journal, 2006, v. 40, n. 9, p. 473, doi. 10.1007/s11094-006-0157-9
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- Article
Allobetulin N-acetylglucosaminide. Synthesis and antimicrobial activity.
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- 2017
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- Publication type:
- Letter
First conjugate of glucuronic acid with triterpenoid dihydrobetulin.
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- 2017
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- Publication type:
- Letter
Synthesis of thiazolylhydrazones of the Stevia rebaudiana glycoside steviolbioside.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 8, p. 1871, doi. 10.1134/S1070363216080168
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- Article
Functionalization of the double bond in the glycoside of the Stevia rebaudiana plant steviolbioside, as a way to macrocyclic glycosides.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 6, p. 1456, doi. 10.1134/S107036321506016X
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- Article
Macrocyclic derivatives of isosteviol with two tetracyclic diterpenoid skeletons.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 2, p. 304, doi. 10.1134/S1070363214020261
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- Article
Hybrid compounds of ent-beyerane diterpenoid isosteviol with pyridinecarboxylic acid hydrazides. Synthesis, structure, and antitubercular activity.
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- Russian Journal of General Chemistry, 2011, v. 81, n. 8, p. 1643, doi. 10.1134/S1070363211080111
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- Article
Studies of isosteviol diterpenoid derivatives by mass spectrometry: II. Fragmentation of isosteviol esters under the electronic impact.
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- Russian Journal of General Chemistry, 2011, v. 81, n. 6, p. 1185, doi. 10.1134/S1070363211060193
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- Article
13-halo derivatives of ent-kauranoic acid. Synthesis and structure.
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- Russian Journal of General Chemistry, 2011, v. 81, n. 5, p. 927, doi. 10.1134/S1070363211050148
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- Article
Reaction of isosteviol diterpenoid with selenium dioxide.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 12, p. 2663, doi. 10.1134/S1070363209120184
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- Article
Synthetic glycosides of ent-caurene series containing substituents with benzyl, phenoxyl, and uracyl fragments.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 12, p. 2668, doi. 10.1134/S1070363209120196
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- Article
Reduction of steviolbioside.
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- 2009
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- Publication type:
- Letter
Mass spectra of isosteviol derivatives: I. Fragmentation of isosteviol derivatives having a Schiff base fragment on C<sup>4</sup> under electron impact.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 11, p. 2377, doi. 10.1134/S1070363209110164
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- Article
O-Alkylation of diterpenoid steviol in the system KOH-DMSO.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 10, p. 2197, doi. 10.1134/S1070363209100193
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- Article
New synthesis of diterpenoid (16 S)-dihydrosteviol.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 5, p. 967, doi. 10.1134/S107036320905017X
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- Article
Isosteviol derivatives having azine and hydrazide fragments.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 8, p. 1356, doi. 10.1134/S1070363207080105
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- Article
First synthetic macrocyclic compounds in the series of ent-beyerane diterpenoids.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 6, p. 1066, doi. 10.1134/S1070363207060205
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- Article
Structure of 16-hydroxyisosteviol-derived dicarboxylic acid esters.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 6, p. 1069, doi. 10.1134/S1070363207060217
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- Article
Alkylation of the isosteviol terpenoid and its oxime with dibromoalkanes in the KOH-DMSO system.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 3, p. 469, doi. 10.1134/S1070363207030218
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- Article
Synthesis of Schiff bases on the basis of the isosteviol terpenoid.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 2, p. 285, doi. 10.1134/S1070363207020168
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- Article
15-Halo-substituted Isosteviols.
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- Russian Journal of General Chemistry, 2005, v. 75, n. 4, p. 583, doi. 10.1007/s11176-005-0276-0
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- Article
Conformation of 1,5-Bis(16-oxobeyeran-19-oyloxy)-3-oxapentane in CCl<sub>4</sub>.
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- Russian Journal of General Chemistry, 2005, v. 75, n. 2, p. 244, doi. 10.1007/s11176-005-0207-0
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- Article
Chemistry and Structure of Diterpenoids: X. Isosteviol Amides.
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- Russian Journal of General Chemistry, 2005, v. 75, n. 2, p. 248, doi. 10.1007/s11176-005-0208-z
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- Article
Chemistry and Structure of Diterpene Compounds of the Kaurane Series: IX. Electrochemical Reactions of Isosteviol and Its Derivatives.
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- Russian Journal of General Chemistry, 2003, v. 73, n. 9, p. 1453, doi. 10.1023/B:RUGC.0000015998.43164.d3
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- Article
Chemistry and Structure of Diterpene Compounds of the Kaurane Series: VII. Chiral Complexes of Isosteviol with Aromatic Compounds.
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- Russian Journal of General Chemistry, 2003, v. 73, n. 8, p. 1249, doi. 10.1023/B:RUGC.0000007650.09032.17
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- Article
Chemistry and Structure of Diterpene Compounds of the Kaurane Series: VIII. Azomethines Derived from Isosteviol.
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- Russian Journal of General Chemistry, 2003, v. 73, n. 8, p. 1255, doi. 10.1023/B:RUGC.0000007651.53262.a5
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- Article
Chemistry and Structure of Diterpene Compounds of the Kaurane Series: VI. Isosteviol Esters.
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- Russian Journal of General Chemistry, 2003, v. 73, n. 7, p. 1119, doi. 10.1023/B:RUGC.0000007623.48416.2b
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- Article
Phosphorylated Glycoconjugates Based on Isosteviol, d-Arabinofuranose, and d-Ribofuranose.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 4, p. 508, doi. 10.1134/S1070428019040158
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- Article
Synthesis and Biological Activity of Alkane-1,1-diylbis(phosphonates) of Diterpenoid Isosteviol.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 1, p. 17, doi. 10.1134/S1070428019010044
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- Article
Synthesis and antitubercular activity of first glucuronosyl phosphates and amidophosphates containing polymethylene chains.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 1, p. 51, doi. 10.1134/S1070428017010092
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- Article
Synthesis of macrocycles on the basis of diterpenoid isosteviol and trehalose.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 10, p. 1488, doi. 10.1134/S1070428015100231
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- Article
Development of synthetic approaches to macrocyclic glycoterpenoids on the basis of glucuronic acid and diterpenoid isosteviol.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 9, p. 1324, doi. 10.1134/S1070428015090201
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- Article
Macrocyclic derivatives of steviolbioside, a glycoside isolated from Stevia Rebaudiana.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 3, p. 424, doi. 10.1134/S1070428015030239
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- Article
Synthetic glycosides containing two isosteviol fragments functionalized with D-glucopyranose.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 4, p. 484, doi. 10.1134/S107042801404006X
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- Article
Wagner-Meerwein rearrangement of steviol 16α,17- and 15α,16-epoxides.
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- Russian Journal of Organic Chemistry, 2010, v. 46, n. 7, p. 1006, doi. 10.1134/S1070428010070080
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- Article
Synthesis and Cytotoxicity Against M-HeLa, HuTu 80, and MCF-7 Human Cancer Cells of the First Nucleoterpenoids of the Isosteviol Diterpenoid Platform.
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- Chemistry of Natural Compounds, 2024, v. 60, n. 6, p. 1061, doi. 10.1007/s10600-024-04520-2
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- Article
Phosphates of the Diterpenoid Isosteviol. Synthesis and Biological Activity<sup>#</sup>.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 4, p. 688, doi. 10.1007/s10600-018-2447-3
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- Article
Synthesis and Antimicrobial and Antituberculosis Activity of the First Conjugates of the Diterpenoid Isosteviol and D-Arabinofuranose.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 1, p. 92, doi. 10.1007/s10600-018-2267-5
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- Article
Synthesis and Antimicrobial Activity of Dihydrobetulin N-Acetylglucosaminides.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 6, p. 1101, doi. 10.1007/s10600-017-2210-1
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- Article
Synthesis and Antimicrobial Activity of Glucuronosyl Derivatives of Steviolbioside from Stevia rebaudiana.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 6, p. 1107, doi. 10.1007/s10600-017-2211-0
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- Article
First Derivative of the Stevia rebaudiana Glycoside Steviolbioside Containing Thiazolylhydrazone Moieties.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 5, p. 870, doi. 10.1007/s10600-016-1798-x
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- Article
Synthesis of the First Macrocyclic Glycoterpenoid Based on Trehalose and the Diterpenoid Isosteviol.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 5, p. 886, doi. 10.1007/s10600-015-1440-3
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- Article
Synthesis of a Macrocyclic Conjugate of the Diterpenoid Isosteviol and Glucuronic Acid.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 4, p. 689, doi. 10.1007/s10600-015-1385-6
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- Article
Open-Chain and Macrocyclic Polyethyleneglycol Esters of the Diterpenoid Isosteviol.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 3, p. 462, doi. 10.1007/s10600-014-0987-8
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- Article
First Conjugates of the Diterpenoid Isosteviol and Glucuronic Acid.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 3, p. 465, doi. 10.1007/s10600-014-0988-7
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- Article
Synthesis of Macrocyclic Derivatives of the Diterpenoid Isosteviol with Two and Four ent-Beyerane Frameworks.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 3, p. 462, doi. 10.1007/s10600-013-0639-4
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- Article
Synthesis and antimicrobial activity of several bis-quaternized ammonium derivatives of the diterpenoid isosteviol.
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- Chemistry of Natural Compounds, 2012, v. 47, n. 6, p. 914, doi. 10.1007/s10600-012-0103-x
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- Article
Synthesis of macrocycles with one and more ent-beyerane skeletons based on the diterpenoid isosteviol.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 3, p. 422, doi. 10.1007/s10600-011-9949-6
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- Article
Synthesis and antituberculosis activity of derivatives of the diterpenoid isosteviol with azine, hydrazide, and hydrazone moieties.
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- Chemistry of Natural Compounds, 2011, v. 47, n. 1, p. 55, doi. 10.1007/s10600-011-9829-0
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- Article