Works matching AU Miftakhov, M.
Results: 171
Structure-biological activity relationship in prostaglandin analogs.
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- Pharmaceutical Chemistry Journal, 2006, v. 40, n. 8, p. 424, doi. 10.1007/s11094-006-0145-0
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UV spectroscopic quantitative determination of methanofullerene derivatives with a different degree of substitution.
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- Journal of Structural Chemistry, 2013, v. 54, n. 4, p. 719, doi. 10.1134/S0022476613040094
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UV spectroscopy of monosubstituted derivatives of 1,2-dihydro-C-fullerenes.
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- Journal of Structural Chemistry, 2012, v. 53, n. 6, p. 1081, doi. 10.1134/S0022476612060091
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Quantitative UV Spectrophotometric Analysis of Mixtures of Substituted C Fullerenes.
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- Journal of Applied Spectroscopy, 2015, v. 82, n. 4, p. 644, doi. 10.1007/s10812-015-0157-1
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13,14-Dehydro-16-phenoxy-PGB<sub>1</sub> Ethyl Esters: Synthesis and Some Properties.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S137, doi. 10.1134/S1070363223140207
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Ring-opening metathesis polymerization (ROMP) of fullerene-containing monomers in the presence of a first-generation Grubbs catalyst.
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- Kinetics & Catalysis, 2017, v. 58, n. 2, p. 111, doi. 10.1134/S0023158417020021
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Transformation of Cloprostenol into E-Type Derivatives and a Comparative Study of Their Uterotonic Activity.
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- Pharmaceutical Chemistry Journal, 2023, v. 57, n. 1, p. 46, doi. 10.1007/s11094-023-02849-6
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Inclusion Complex of 11-deoxymisoprostol and Glycyrrhizic Acid with Improved Anti-Ulcer Activity.
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- Pharmaceutical Chemistry Journal, 2022, v. 56, n. 5, p. 607, doi. 10.1007/s11094-022-02684-1
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Features of mass and charge transport to gas discharge plasma from aqueous sodium chloride solution serving as a cathode.
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- High Energy Chemistry, 2018, v. 52, n. 1, p. 99, doi. 10.1134/S0018143918010149
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- Article
Methyl 5-[Di(1H-pyrrol-2-yl)methyl]-3,4-dimethoxythiophene-2-carboxylate in Approaches to New Thienopyrroles.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 12, p. 2512, doi. 10.1134/S1070428024120273
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Synthesis of the C<sup>1</sup>–C<sup>9</sup> Block of Epothilone D Analogue.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 12, p. 2367, doi. 10.1134/S1070428024120091
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Synthesis of (Carboxymethylidene)cyclopentenedione Derivatives via the Oxidative Cleavage of the Allylic Double Bond in 2-Allyl-2,4-dichloro-5-(2,4,6-trimethoxyphenyl)cyclopent-4-ene-1,3-dione.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 11, p. 2298, doi. 10.1134/S1070428024110186
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Pd(PPh<sub>3</sub>)<sub>4</sub>-Catalyzed Elimination of Acetic Acid from (±)-9α,11α,15α-Triacetoxycloprostenol 4-Methoxybenzyl Ester.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 10, p. 1892, doi. 10.1134/S1070428024100026
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Synthesis of a Misoprostol Analogue, 11-Deoxy-13,14-didehydro-17-methyl-20-norprostaglandin B<sub>1</sub> Ethyl Ester.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 9, p. 1681, doi. 10.1134/S1070428024090094
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Synthesis of (±)-Entecavir.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 3, p. 410, doi. 10.1134/S1070428024030060
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Reaction of Derivatives of the [2+2]-Cycloadduct of Dichloroketene and Dimethylfulvene with Ozone.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 2, p. 349, doi. 10.1134/S1070428024020180
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Synthesis of (S)-N-Ethyl-2-(5-methylidene-4-oxocyclopent-2-en-1-yl)acetamide―A Model exo-Methylidenecyclopentenone Bioisoster of Prostamides.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 2, p. 231, doi. 10.1134/S1070428024020076
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Double Acylation Product in the SnCl<sub>4</sub>-promoted Reaction of 4,5-Dichlorocyclopent-4-en-1,3-dione with 1,3,5-Trimethoxybenzene.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 8, p. 1449, doi. 10.1134/S1070428023080201
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Acid-Catalyzed Acetonation of D-Ribose.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 4, p. 581, doi. 10.1134/S1070428023040048
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Synthesis of New 1,3,4-Oxadiazole and 1,2,3-Triazole Derivatives of Thieno[3,2-b]pyrrolecarboxylic Acid.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 2, p. 328, doi. 10.1134/S107042802302015X
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Synthesis of (3S,4S)-4-Acetyl-3-(1R)-1-hydroxyethyl-1-(4-methoxyphenyl)azetidin-2-one.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 11, p. 1676, doi. 10.1134/S1070428022110203
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Zinc-promoted Reactions of (2Z,E)-[2-Aryl(hetaryl)methylidene]-4-chloro-5-phenyl(2,4,6-trimethoxyphenyl)cyclopent-4-ene-1,3-diones with Methyl Bromoacetate.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 11, p. 1668, doi. 10.1134/S1070428022110185
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Synthesis of a C<sup>3</sup> Hydroxyproline-modified Carbapenem.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 11, p. 1664, doi. 10.1134/S1070428022110173
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Synthesis of 2-(16,17-Epoxy-3β,20-dihydroxypregn-5-en-20-yl)-1,3-dithiane from Diosgenin.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 11, p. 1641, doi. 10.1134/S1070428022110124
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Synthesis of Propargyl (±)-(5-Methylidene-4-oxopent-2-en-1-yl)Acetate.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 11, p. 1623, doi. 10.1134/S1070428022110094
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Synthesis of the 2,3-Asyridinyl Derivative of d-Carvone.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 5, p. 724, doi. 10.1134/S107042802205013X
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Synthesis of Ethyl Ethers 13,14-Dehydro-16-aryloxy-11-deoxyprostaglandin E<sub>1</sub>.
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- Russian Journal of Organic Chemistry, 2022, v. 58, n. 5, p. 691, doi. 10.1134/S1070428022050086
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Reactions of 2,3-Dibromo-2-methylpropanamides Promoted by Potassium tert-Butoxide.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 10, p. 1643, doi. 10.1134/S1070428021100122
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β-Lactam Ring Opening in the Reformatsky Reaction of (3R,4R)-4-Acetoxy-3-((1R)-1-{[tert-butyl(dimethyl)silyl]oxy}ethyl)azetidin-2-one with Ethyl 4-Bromo-3-oxopentanoate.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 9, p. 1461, doi. 10.1134/S1070428021090116
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Synthesis of a New 10,11-Didehydro Analog of Epothilone D.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 6, p. 889, doi. 10.1134/S1070428021060038
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Aromatic and Heteroaromatic 4-Benzyl-4H-thieno[3,2-b]pyrrole-5-carbohydrazides.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 1, p. 117, doi. 10.1134/S1070428021010176
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Regioselective Intermolecular Cyclization of Methyl (E)-3-[(4S,5S)-5-Acetyl-2,2-dimethyl-1,3-dioxolan-4-yl)]prop-2-enoate.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 11, p. 2043, doi. 10.1134/S1070428020110226
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New Carboxamides of the Thieno[3,2-b]pyrrole Series.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 10, p. 1850, doi. 10.1134/S1070428020100309
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4H-Thieno[3,2-b]pyrrole-5-carbohydrazides and Their Derivatives.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 9, p. 1545, doi. 10.1134/S1070428020090079
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Novel 13,14-Dehydro Analogs of Prostaglandins of the 11-Deoxy Series.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 8, p. 1347, doi. 10.1134/S1070428020080035
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Synthesis and Isomerization of the 2-Methyl Enal Fragment of Acyclic Precursors to 9,11-Diene Analogs of Epothilones.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 7, p. 1140, doi. 10.1134/S1070428020070039
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Synthesis of Dicobalt Hexacarbonyl Complex with B-Type 13,14-Didehydromisoprostol Analog.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 4, p. 708, doi. 10.1134/S1070428020040211
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Synthesis of 13,14-Dehydro-15-deoxy-16-hydroxy-16-methyl-17-phenoxyprostaglandin B1 Ethyl Ester.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 3, p. 540, doi. 10.1134/S1070428020030288
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1,8-Diazabicyclo[5.4.0]undec-7-ene-Promoted Oxidation by Atmospheric Oxygen of an Allylsilane Derived from γ-Formyl-Substituted Cyclopentene.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 2, p. 255, doi. 10.1134/S1070428020020128
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Synthesis of C3-Modified Carbapenems.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 1, p. 7, doi. 10.1134/S1070428020010029
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- Article
New 4-Substituted 5-(1H-Pyrrol-2-ylmethyl)-4H-thieno[3,2-b]pyrroles and Their Reactions with N-Bromosuccinimide.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 12, p. 1907, doi. 10.1134/S1070428019120169
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4H-Thieno[3,2-b]pyrrole-5-carboxylate Conjugates with Taurine and Its Tetrabutylammonium Salt.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 12, p. 1902, doi. 10.1134/S1070428019120157
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New Differently Functionalized Cyclopentenediones.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 12, p. 1869, doi. 10.1134/S1070428019120091
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Low-Temperature Reactions of α-Bromopropanoyl Chloride with Lithium Derivative of Ethyl Acetate.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 11, p. 1726, doi. 10.1134/S1070428019110137
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New 11,13-Dienone Analog of Cloprostenol.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 10, p. 1465, doi. 10.1134/S1070428019100038
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Yamaguchi Esterification in the Synthetic Approaches to Precursors of Epothilone D Analogs.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 9, p. 1439, doi. 10.1134/S1070428019090264
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New Key Building Block for Ixabepilone from R-(-)-Carvone.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 9, p. 1370, doi. 10.1134/S1070428019090161
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Chiral 7-Oxabicyclo[2.2.1]heptane Building Blocks for Prostanoids.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 8, p. 1131, doi. 10.1134/S1070428019080116
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Synthetic Approaches to 15-Deoxy-Δ<sup>12,14</sup>-prostaglandin J<sub>2</sub>. A New Key Building Block Based on (3aR,6R,6aS)-6-Trimethylsilyl)-3,3a,6,6a-tetrahydro-1H-cyclopenta[c]furan-1-one.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 6, p. 831, doi. 10.1134/S1070428019060137
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ω-Aryloxy Analogs of Prostamides.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 4, p. 498, doi. 10.1134/S1070428019040134
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