Works matching IS 10704280 AND DT 2021 AND VI 57 AND IP 12
Results: 28
Three-Component Reaction of 1H-Pyrrole-2,3-diones with Malononitrile and Phthalhydrazide.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2077, doi. 10.1134/S1070428021120289
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Synthesis of Spiro[[1,2,5]oxadiazolo[3,4-b]pyrazine-5,2′-pyrroles] by Reaction of Pyrrolooxazinetriones with Diaminofurazan.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2074, doi. 10.1134/S1070428021120277
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Synthesis of 4-[(3,3-Dimethyl-3,4-dihydroisoquinolin-1-yl)sulfanyl]anilines by the Ritter Reaction.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2071, doi. 10.1134/S1070428021120265
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Synthesis of 2-[(Pyrrol-2-yl)sulfanyl]acetic Acids by Reaction of Pyrrolo[2,1-c][1,4]oxazinetriones with 2-Sulfanylacetic Acid.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2067, doi. 10.1134/S1070428021120253
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Reaction of 4,5-Diaroyl-1H-pyrrole-2,3-diones with Thiosemicarbazide. Synthesis of 1H-Pyrazole-5-carboxamides.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2063, doi. 10.1134/S1070428021120241
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Synthesis and Molecular Docking Study of Arylsulfanyl Pyrazolylpyrazoline Derivatives as Antitubercular Agents.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2054, doi. 10.1134/S107042802112023X
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Ultrasound-Mediated Synthesis of Sulfonyl Urea Derivatives and Their In Vitro Antiproliferative Activity.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2048, doi. 10.1134/S1070428021120228
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Synthesis and In Vitro Anticancer Activity of Triazolyl Analogs of Podophyllotoxin, a Naturally Occurring Lignin.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2039, doi. 10.1134/S1070428021120216
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Synthetic Development and Assessment of Antioxidant Activity of Imino[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile and Its Derivatives.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2031, doi. 10.1134/S1070428021120204
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One-Pot Multicomponent Synthesis, Molecular Docking, and In Vitro Antibacterial Activities of 1-{(Aryl)[(5-methyl-1,3-thiazol-2-yl)amino]methyl}naphthalen-2-ol.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2024, doi. 10.1134/S1070428021120198
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Synthesis, Crystal Structure, and Spectral Study of a NovelIndenoimidazole Carboxylic Acid Amide.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2018, doi. 10.1134/S1070428021120186
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Copper-Catalyzed Oxidative Cascade Cyclization of Activated Alkenes with Azobis Compounds: Access to Cyano-Substituted Benzimidazo[2,1-a]isoquinolin-6(5H)-ones.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2010, doi. 10.1134/S1070428021120174
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- Article
Sulfonamide-Functionalized Porous Organic Framework as an Efficient Heterogeneous Acid Catalyst for One-Pot Preparation of 1,8-Dioxooctahydroxanthenes.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 2002, doi. 10.1134/S1070428021120162
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New Thiazole-Bearing Oxadiazole Derivatives: Synthesis, Thymidine Phosphorylase Inhibitory Potential, and Molecular Docking Study.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1993, doi. 10.1134/S1070428021120150
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- Article
Synthesis of Glycoluril using Urea Phosphate.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1988, doi. 10.1134/S1070428021120149
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Synthesis and Some Properties of 2-(Furan-2-yl)[1,3]thiazolo[4,5-b]pyridine.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1983, doi. 10.1134/S1070428021120137
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Synthesis and Properties of 1-(Alkylsulfanyl)-3-(morpholin-4-yl)propan-2-yl Arylcarbamates and Arylcarbamothioates.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1979, doi. 10.1134/S1070428021120125
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- Article
Synthesis and Antibacterial Activity of N-Substituted 2-(Benzylimino)-4-styryl-2,5-dihydrofuran-3-carboxamides.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1974, doi. 10.1134/S1070428021120113
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Synthesis of 4,5-Dialkyl-2-perfluoroaryl-1H-imidazol-1-ols and 4,5-Dimethyl-2-perfluoroaryl-1H-imidazoles.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1968, doi. 10.1134/S1070428021120101
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Synthesis and Luminescence Spectral Properties of New Cyano-Substituted 2,2′-Bipyridine Derivatives.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1961, doi. 10.1134/S1070428021120095
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Synthesis, Intramolecular Cyclization, and Antinociceptive Activity of Substituted 2-[2-(4-Nitrobenzoyl)hydrazinylidene]-4-oxobut-2-enoic Acids.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1955, doi. 10.1134/S1070428021120083
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Multicomponent Synthesis of 1,3-Bis[(alkylsulfanyl)methyl]-1,3,5-triazinan-2-ones.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1948, doi. 10.1134/S1070428021120071
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Synthesis and Physicochemical Properties of New Chalcones Containing a 2-Chloroimidazo[1,2-a]pyridine Fragment.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1940, doi. 10.1134/S107042802112006X
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Synthesis of Highly Functionalized Biologically Active Tetracyclic Diterpenoids from ent-Kaur-16-en-19-oic Acid under Modified Prévost-Woodward Reaction Conditions.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1931, doi. 10.1134/S1070428021120058
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Convenient Synthesis of Symmetrical Polyfluorinated Diphenyl Sulfides.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1921, doi. 10.1134/S1070428021120046
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Synthesis and Properties of N,N′-Disubstituted Ureas and Their Isosteric Analogs Containing Polycyclic Fragments: XIII. N-[(3-Bromoadamantan-1-yl)methyl]ureas and Symmetrical Diureas.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1913, doi. 10.1134/S1070428021120034
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Mass Spectra of New Heterocycles: XXIII. Electron Impact and Chemical Ionization Study of 5-[(Cyanomethyl)sulfanyl]- and 5-[(1,3-Dioxolan-2-ylmethyl)sulfanyl]-1H-pyrrol-2-amines.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1901, doi. 10.1134/S1070428021120022
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Synthesis and Properties of N,N′-Disubstituted Ureas and Their Isosteric Analogs Containing Polycyclic Fragments: XII. N-(1,3,3-Trimethylbicyclo[2.2.1]heptan-2-yl)-N′-R-ureas and -thioureas.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 12, p. 1891, doi. 10.1134/S1070428021120010
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