| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allylation of (R)-2,3-O-Cyclohexylideneglyceraldehyde with 2-Substituted Allylstannanes. Application in the Synthesis of Natural Compounds
|
Varanchuk, V. V.
|
|
|
61 |
4 |
p. 602-615
|
artikel
|
| 2 |
4-Aryl-3-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-phenyl-1H-pyrazoles: Synthesis, Characterization, and Biological Activity
|
Rechel, P. A.
|
|
|
61 |
4 |
p. 743-748
|
artikel
|
| 3 |
Base-Catalyzed One-Pot Synthesis of Tetrahydrofuropyridinone Derivatives. Antioxidant and Molecular Docking Studies
|
Sadaria, N.
|
|
|
61 |
4 |
p. 721-730
|
artikel
|
| 4 |
Design, Synthesis, and Antitumor Activity of Erianin Derivatives
|
Jiang, Bailing
|
|
|
61 |
4 |
p. 731-742
|
artikel
|
| 5 |
Design, Synthesis, and Characterization of Novel 3-(2-Amino-6-arylpyrimidin-4-yl)-1-methylquinolin-2(1H)-one Derivatives and Screening for Their Antioxidant and Acetylcholinesterase Inhibitory Potency
|
Sujatha, M. L.
|
|
|
61 |
4 |
p. 696-705
|
artikel
|
| 6 |
Erratum to: Synthesis of Bi- and Tricyclic Monoesters of Dicarboxylic Acids
|
Mamedov, M. K.
|
|
|
61 |
4 |
p. 764
|
artikel
|
| 7 |
Fe3O4@Sal@Cu as a Novel Multifunctional Magnetic Nanocatalyst for Clean and Mild Synthesis of 2,3-Dihydro-1H-perimidines
|
Ferdosian, R.
|
|
|
61 |
4 |
p. 689-695
|
artikel
|
| 8 |
Green Solvent-Free Synthesis of Biologically Relevant Heterocycles—A Mini Review
|
Dinodia, M.
|
|
|
61 |
4 |
p. 675-688
|
artikel
|
| 9 |
Heterocyclization of 2-Acetylcyclopentanone
|
Danagulyan, G. G.
|
|
|
61 |
4 |
p. 571-579
|
artikel
|
| 10 |
One-Pot Synthesis of Bicyclo[2.2.1]heptane Derivatives by Three-Component Coupling of Norbornene, Aryl Halides, and Arylacetylenes in the Presence of Ligand-Free Palladium Catalytic Systems
|
Larina, E. V.
|
|
|
61 |
4 |
p. 647-654
|
artikel
|
| 11 |
Reaction of Fluorodinitroacetonitrile with Nitrile Oxides
|
Tyrkov, A. G.
|
|
|
61 |
4 |
p. 760-763
|
artikel
|
| 12 |
Regioselective Synthesis of Furocoumarin Derivatives and Their Docking and ADME Studies for Alzheimer’s Disease
|
Lokhande, M. N.
|
|
|
61 |
4 |
p. 749-759
|
artikel
|
| 13 |
Substituted Ureas and Their Analogs Containing Cage Fragments: II. N,N′-(4-(Adamantan-1-yl)-1,2-phenylene)bis[N′-(R-phenyl)ureas and -thioureas]
|
Zapravdina, D. M.
|
|
|
61 |
4 |
p. 580-586
|
artikel
|
| 14 |
Synthesis and Optical Properties of 6-Alkylamino-2-amino-4-[(4-(dimethylamino)phenyl]pyridine-3,5-dicarbonitriles
|
Ramskaya, E. N.
|
|
|
61 |
4 |
p. 640-646
|
artikel
|
| 15 |
Synthesis, Antimicrobial Activity, and Molecular Docking of Phenylcarbamate Derivatives Containing a Heterocyclic Fragment
|
Velikorodov, A. V.
|
|
|
61 |
4 |
p. 625-634
|
artikel
|
| 16 |
Synthesis of (2E,4E)-2-(4-Aryl-1,3-selenazol-2-yl)-5-phenylpenta-2,4-dienenitriles
|
Frolov, K. A.
|
|
|
61 |
4 |
p. 621-624
|
artikel
|
| 17 |
Synthesis of 6-(1H-Pyrrol-1-yl)azolo[1,5-a]pyrimidin-7-amines by the Clauson–Kaas Reaction
|
Fedotov, V. V.
|
|
|
61 |
4 |
p. 660-668
|
artikel
|
| 18 |
Synthesis of Ionic Liquids Based on N-(Aminopropyl)imidazolium Salts
|
Dorofeev, I. A.
|
|
|
61 |
4 |
p. 655-659
|
artikel
|
| 19 |
Synthesis of New (2E,4E)-2-Cyano-5-phenylpenta-2,4-dienethioamide Derivatives
|
Frolov, K. A.
|
|
|
61 |
4 |
p. 616-620
|
artikel
|
| 20 |
Synthesis of Principal Building Blocks of Amphidinolides of the G and H Families
|
Mineyeva, I. V.
|
|
|
61 |
4 |
p. 587-601
|
artikel
|
| 21 |
Synthesis of Substituted 2-Arylimino-3-oxopropanenitriles and 2-(Arylimino)propanedinitriles by Oxidative Coupling of Primary Aromatic Amines with Aroylacetonitriles and Malononitrile
|
Kachanov, A. V.
|
|
|
61 |
4 |
p. 669-674
|
artikel
|
| 22 |
Ultrasound-Assisted Green Synthesis of Diversely Functionalized Pyrido[2,3-c]coumarins Catalyzed by Graphene Oxide Nanosheets under Solvent-Free Ambient Conditions
|
Kausar, N.
|
|
|
61 |
4 |
p. 706-720
|
artikel
|
| 23 |
Unexpected Formation of Allylic Hydroxylation Product in the Ozonolysis of N-[2-(Cyclohex-1-en-1-yl)-6-methylphenyl]-4-methylbenzenesulfonamide
|
Safargalin, R. R.
|
|
|
61 |
4 |
p. 635-639
|
artikel
|
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