Works matching AU Burilov, A. R.
Results: 127
Synthesis and Structure of Hybrid Compounds Based on Phosphoryl Acetic Acid Hydrazide, Isatin, and Sterically Hindered Phenols.
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- Journal of Structural Chemistry, 2019, v. 60, n. 11, p. 1804, doi. 10.1134/S0022476619110143
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- Article
Reactions of derivatives of phosphorylacetic acid hydrazides with 3,5-di-tert-butyl-4-hydroxybenzyl acetate.
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- Synthetic Communications, 2020, v. 50, n. 1, p. 41, doi. 10.1080/00397911.2019.1681453
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- Article
Synthesis of substituted ureas possessing alkyl aromatic fragments via the reaction of 1-(3,3-diethoxypropyl)ureas with phenols.
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- Synthetic Communications, 2018, v. 48, n. 19, p. 2545, doi. 10.1080/00397911.2018.1512000
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- Article
Acid-catalyzed intramolecular cyclization of N -(4,4-diethoxybutyl)sulfonamides as a novel approach to the 1-sulfonyl-2-arylpyrrolidines.
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- Synthetic Communications, 2017, v. 47, n. 1, p. 44, doi. 10.1080/00397911.2016.1249288
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- Article
Synthesis and investigation of antimicrobial activity of compounds derived from benzo[C][1,2,5]oxadiazole-1-oxides and phenolates.
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- Synthetic Communications, 2016, v. 46, n. 18, p. 1560, doi. 10.1080/00397911.2016.1213295
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- Article
Acid-Catalyzed Reaction of (4,4-Diethoxybutyl)ureas with Phenols as a Novel Approach to the Synthesis of α -Arylpyrrolidines.
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- Synthetic Communications, 2015, v. 45, n. 10, p. 1215, doi. 10.1080/00397911.2015.1011340
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- Article
Highly Diastereoselective Synthesis of 2‐Arylpyrrolidine Derivatives via the Crystallization‐induced Diastereomer Transformation.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 1, p. 1, doi. 10.1002/ajoc.202100687
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- Article
2‐(Het)aryl‐N‐phosphorylpyrrolidines via Cyclization of Phosphorus Acid Amides: A Regioselective Approach.
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- ChemistrySelect, 2020, v. 5, n. 39, p. 12045, doi. 10.1002/slct.202003353
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- Article
Reactions of 1‐(3,3‐Diethoxypropyl)urea with Phenols: Synthesis of 1,6‐Disubstituted Tetrahydropyrimidine‐2(1H)‐ones.
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- ChemistrySelect, 2019, v. 4, n. 37, p. 11038, doi. 10.1002/slct.201902754
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- Article
Acid‐Catalyzed Cascade Reaction of 4‐Aminobutanal Derivatives with (Hetero)aromatic Nucleophiles: A Versatile One‐Pot Access to 2‐(Hetero)arylpyrrolidines.
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- ChemistrySelect, 2019, v. 4, n. 32, p. 9322, doi. 10.1002/slct.201902011
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- Article
Norhygrine Alkaloid and Its Derivatives: Synthetic Approaches and Applications to the Natural Products Synthesis.
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- Helvetica Chimica Acta, 2022, v. 105, n. 1, p. 1, doi. 10.1002/hlca.202100158
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- Article
Synthesis of unsymmetrical cage phosphonates from heterocyclic systems based on 2H-1,2-benzoxaphosphinine.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 12, p. 1605, doi. 10.1007/s10593-020-02856-5
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- Article
Synthesis of Novel 2-Hetarylpyrrolidines via the Reaction of N-(4,4-diethoxybutyl)amidophosphates with C-nucleophiles.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 10, p. 1363, doi. 10.1007/s10593-020-02823-0
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- Article
Correction to: Synthesis of novel macrocyclic and heterocyclic taurine derivatives based on the reaction of sodium 2-[(4,4-diethoxybutyl)amino]ethanesulfonate with phenols.
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- 2020
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- Correction Notice
Synthesis of novel macrocyclic and heterocyclic taurine derivatives based on the reaction of sodium 2-[(4,4-diethoxybutyl)amino]ethanesulfonate with phenols.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 888, doi. 10.1007/s10593-020-02746-w
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- Article
One-Pot Synthesis of N-(Phosphorylmethyl)Pyrrolidines via Acid-Catalyzed Cascade Elimination/Cyclization/Friedel–Crafts Reaction.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 5, p. 542, doi. 10.1007/s10593-020-02697-2
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- Article
Reactions of pyridoxal with aromatic diamines.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 3, p. 326, doi. 10.1007/s10593-020-02663-y
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- Article
Hydroxylammonium Sulfate: A New Transformer of Ethers and Phosphorus Pentachloride Adducts.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S583, doi. 10.1134/S1070363223150239
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- Article
O-Alkyl-3,5-di-tert-butyl-4-hydroxybenzylchlorophosphonates in the Synthesis of New Phosphonamidates Containing Sterically Hindered Phenolic and N-Heterocyclic Fragments.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S577, doi. 10.1134/S1070363223150227
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- Article
Synthesis of A New Imidazocoumarin by Reaction of 1-Methyl-3-phenyl-1,3-dihydro-2H-imidazol-2-one with 4,6-Di-tert-butyl-3-(methoxymethyl)benzene-1,2-diol.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S510, doi. 10.1134/S1070363223150136
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- Article
Unusual Reduction of Benzofuroxans to Benzofurazans with the Participation of the Terminal Amino Group.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S491, doi. 10.1134/S1070363223150112
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- Article
Synthesis of New Symmetrical Diamidophosphates Based on meta-Phenylenediamine under Microwave Irradiation.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 6, p. 1386, doi. 10.1134/S1070363223060099
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- Article
Synthesis of New Imidazolidin-2-ones Based on the Reaction of 1-(2,2-Dimethoxyethyl)urea with C-Nucleophiles.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 6, p. 1322, doi. 10.1134/S1070363223060026
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- Article
Synthesis of Novel Tetrahydropyrimidines via the Reaction of Sodium [1-(3,3-Diethoxypropyl)ureido]methanesulfonates with C-Nucleophiles.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 3, p. 495, doi. 10.1134/S1070363223030052
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- Article
New Bromine-Containing Symmetrical and Unsymmetrical Cage Phosphonates.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 7, p. 1246, doi. 10.1134/S1070363222070118
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- Article
Synthesis of New Furopyridines Containing Carbonyl Group in Alkyl Substituent.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 7, p. 1241, doi. 10.1134/S1070363222070106
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- Article
Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 2, p. 161, doi. 10.1134/S1070363222020049
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- Article
Octacis(2-hydroxyethylated) Calix[4]resorcinarenes Phosphorochloridates as Precursors in Production of Water-Soluble Calix[4]resorcinarene and Phosphoramidates.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 10, p. 2038, doi. 10.1134/S1070363221100170
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- Article
Some Features of Phosphorylation and Benzoylation of Pyridoxal Imidazolidines.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 9, p. 1667, doi. 10.1134/S1070363221090097
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- Article
Reactions of Pyridoxal Derivatives with Phenyl Iso(thio)cyanates.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 8, p. 1431, doi. 10.1134/S1070363221080016
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- Article
Synthesis of New Diaryl(hetaryl)ethylphosphonic Acids.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 7, p. 1420, doi. 10.1134/S1070363221070215
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- Article
Unsymmetrical Pyridoxal-Based Bisazomethines.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 7, p. 1265, doi. 10.1134/S1070363221070021
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- Article
Synthesis of New C-Alkyl-N-pyridoxylmethylbenzimidazoles.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 9, p. 1756, doi. 10.1134/S1070363220090261
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- Article
Synthesis of New α-Aminophosphonates Based on Cyclohexylamine.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 6, p. 1100, doi. 10.1134/S1070363220060274
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- Article
Pyridoxal Azomethine Salts.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 11, p. 2185, doi. 10.1134/S1070363219110033
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- Article
Synthesis of 2-(Diphenylphosphoryl)pyrrolidine-1-carboxamides Based on the Reaction of 1-(4,4-Diethoxybutyl)ureas with Diphenyl Chlorophosphine.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 10, p. 2143, doi. 10.1134/S1070363219100244
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- Article
Synthesis of Alkylphosphoryl-Containing 4(5)-Arylimidazolin-2-ones.
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- 2019
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- Publication type:
- Letter
1-(3,3-Diethoxypropyl)-1-[(dihexylphosphoryl)methyl]-3-phenylurea in the Synthesis of 4-Aryl-Substituted Tetrahydropyrimidin-2-ones.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 11, p. 2442, doi. 10.1134/S1070363218110312
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- Article
2H-Benzo[e]-1,2-oxaphosphorine Related Heterocycles as Precursors for the Synthesis of Unsymmetrical Bicyclic Phosphonates.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1941, doi. 10.1134/S1070363218090323
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- Article
Synthesis of 2-Arylpyrrolidines by Reactions of 3-Arylidene-1-pyrrolines with Phenols.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1934, doi. 10.1134/S107036321809030X
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- Article
Reactions of Pyridoxal with Heterocycles Containing Primary Amino Group.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1918, doi. 10.1134/S1070363218090268
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- Article
Kabachnik-Fields Reaction in the Synthesis of New Acetal-Containing Aminophosphine Oxides.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1912, doi. 10.1134/S1070363218090244
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- Article
Pyridoxal: A New Alkylating Agent in Reactions with Phenols and Polyphenols.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1832, doi. 10.1134/S1070363218090116
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- Article
New Furopyridines Containing Pyridoxal and Pyrazolone Fragments.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1818, doi. 10.1134/S1070363218090098
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- Article
Synthesis and Some Reactions of New Acetals Containing Aminoethylenephosphoryl Fragment.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 147, doi. 10.1134/S1070363218010267
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- Article
Phosphorylation of Oxyethylated Calix[4]resorcinols with Phosphorous Acid Amides.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 143, doi. 10.1134/S1070363218010255
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- Article
New Bicyclic Phosphonates with Benzyl Fragments.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 140, doi. 10.1134/S1070363218010243
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- Article
Reaction of 4-Chloro-6-[1-(vinylsulfonyl)pyrrolidin-2-yl]benzene-1,3-diol with Some Amines.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 131, doi. 10.1134/S107036321801022X
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- Article
Azomethines Based on Pyridoxal-Derived Aromatic Aldehydes.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 1, p. 41, doi. 10.1134/S1070363218010073
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- Article
Phosphorus-containing azomethines based on salicylaldehyde and thiosemicarbazide.
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- Russian Journal of General Chemistry, 2013, v. 83, n. 10, p. 1963, doi. 10.1134/S1070363213100307
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- Article