Zobrazeno 1 - 10 of 13 pro vyhledávání: '"M. E. Mironov"'
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Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety
Autor: T. G. Tolstikova, Tatyana V. Rybalova, M. E. Mironov, A. I. Poltanovich, M. P. Dolgikh, Elvira E. Shults
Publikováno v: Russian Chemical Bulletin. 69:537-546
Conjugates of terpenoids with 1,3,5-trisubstituted pyrazoles were synthesized by the cross-coupling of methyl 16-(2-chloro-2-oxoacetyl)labdatrienoate with terminal arylacetylenes via the Castro—Stephens reaction and heterocyclization of arylalkyne-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2fde2d2e8adbf144cb2eace1dcff4dda
https://doi.org/10.1007/s11172-020-2795-6
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3
Copper-catalyzed 1,3-dipolar cycloaddition reaction of spirosolanederived azide for the preparation of modified solasodine alkaloid
Autor: M. E. Mironov, Anna B. Skorova, Anastasiya O. Finke, Elvira E. Shults
Publikováno v: Chemistry of Heterocyclic Compounds. 54:411-416
Modification of the steroidal alkaloid solasodine was performed by introduction of 1,2,3-triazolyl substituents at the С-6 atom of spirosolane ring system. The azidolysis of 5,6α-epoxysolasodine diacetate, formed as the major product during epoxida
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ef808d8d2bc316e433a7f19007abf6ee
https://doi.org/10.1007/s10593-018-2284-0
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5
Synthesis of 3-trimethylsiloxy-1-(furan-3-yl)butadiene and its reactions with dienophiles
Autor: M. E. Mironov, Elvira E. Shults, Irina Yu. Bagryanskaya
Publikováno v: Chemistry of Heterocyclic Compounds. 52:364-373
3-Trimethylsilyloxy-1-(furan-3-yl)butadiene was synthesized and studied in reactions with 2,2-dimethyl-5-methylidene-1,3-dioxane-4,6-diones, 5-methylenepyrimidine-2,4,6-triones, as well as with imines. Reactions with dienophiles containing an exo-met
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e649834da181279a1cf410f1c71955d2
https://doi.org/10.1007/s10593-016-1897-4
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6
Furanolabdanoid-based 1,2,4-oxadiazoles: Synthesis and cytotoxic activity
Autor: Makhmut M. Shakirov, Andrey G. Pokrovsky, Elvira E. Shults, Yurii V. Kharitonov, Mikhail A. Pokrovsky, M. E. Mironov
Publikováno v: ChemistrySelect. 1:417-424
Several 15,16-epoxy-8,13,14-labdatriene derivatives modified at the C-16 position with a 1,2,4-oxadiazole ring with various substituent in the 5-th position, were obtained via multistep synthesis from 16-formyl derivatives of natural diterpenoid lamb
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e1a90fa7fb330c642d4985d6df66c286
https://doi.org/10.1002/slct.201600042
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7
Furanoditerpenoids of the Labdane Series: Occurrence in Plants, Total Synthesis, Several Transformations, and Biological Activity
Autor: E. E. Shul′ts, Yu. V. Kharitonov, M. E. Mironov
Publikováno v: Chemistry of Natural Compounds. 50:2-21
Structures of plant furanolabdanoids and synthetic schemes for a series of furanolabdanoids (coronarins A and E, hedychenone, acuminolide and 17-O-acetylacuminolide) from the available diterpenoids sclareol and larixol were reviewed. Attention was fo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0fbcf53dc903dc0e60fb0734a0d984d0
https://doi.org/10.1007/s10600-014-0861-8
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8
6-(4′-Aryl-1′,2′,3′-triazolyl)-spirostan-3,5-diols and 6-(4′-Aryl-1′,2′,3′-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Autor: Sergey V. Cheresis, Olga S. Oleshko, Vladislav K. Pechurov, Tatyana V. Rybalova, M. A. Pokrovskii, Elvira E. Shults, M. E. Mironov, V. V. Stupak, A. G. Pokrovskii, S. V. Mishinov
Publikováno v: Steroids. 151:108460
In an endeavour to develop potent anti-tumor agents from diosgenin, a series of C-6 derived 1,2,3-triazolyl derivatives were designed and synthesized by employing Cu(I) catalyzed Huisgen 1,3-dipolar cycloaddition reaction of novel azides – (22R,25R
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86fcba166e0f859568dbd371d24b2bc0
https://doi.org/10.1016/j.steroids.2019.108460
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9
ChemInform Abstract: Furanolabdanoid-Based 1,2,4-Oxadiazoles: Synthesis and Cytotoxic Activity
Autor: Elvira E. Shults, M. E. Mironov, Yurii V. Kharitonov, Andrey G. Pokrovsky, Makhmut M. Shakirov, Mikhail A. Pokrovsky
Publikováno v: ChemInform. 47
Several 15,16-epoxy-8,13,14-labdatriene derivatives modified at the C-16 position with a 1,2,4-oxadiazole ring with various substituent in the 5-th position, were obtained via multistep synthesis from 16-formyl derivatives of natural diterpenoid lamb
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ffe946d57023e85da077c543737989a
https://doi.org/10.1002/chin.201626212
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10
Synthetic transformations of higher terpenoids: XXIII. Synthesis of diterpenoid-based dihydroisoindolones
Autor: M. E. Mironov, Yu. V. Kharitonov, Makhmut M. Shakirov, Elvira E. Shults, Tolstikov Genrikh A, Yu. V. Gatilov
Publikováno v: Russian Journal of Organic Chemistry. 46:1869-1882
Vilsmeier-Haak reaction of phlomisoic acid methyl ester gave a mixture of 15- and 16-formyllabdanoids. In addition, methyl 2-formyldodecahydrophenanthro[1,2-b]furan-6-carboxylate was isolated, and its structure was determined by X-ray analysis. Reduc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::530dbd29aab3cb1828591221aae8b32c
https://doi.org/10.1134/s107042801012016x
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