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European Journal of Organic Chemistry, ISSN 1434-193X, 07/2016, Volume 2016, Issue 20, pp. 3282 - 3299
In this review we present recent advances in C–H bond activation for transition‐metal‐catalyzed acyloxylation. This activation is a powerful method for the... 
C–H activation | Synthetic methods | Palladium | Oxygenation | Homogeneous catalysis | ROOM-TEMPERATURE | C-H BOND | CHEMISTRY, ORGANIC | FORMING REDUCTIVE ELIMINATION | C-H activation | ORTHO-ACETOXYLATION | COUPLING REACTIONS | TETHERED DIRECTING GROUP | OXIDATIVE ACYLOXYLATION | ORTHO-BENZOXYLATION | PALLADIUM(IV) COMPLEXES | CARBOXYLIC-ACIDS
Journal Article
Medicinal Chemistry Research, ISSN 1054-2523, 7/2019, Volume 28, Issue 7, pp. 974 - 983
In this manuscript, 17 aminoalkyl-substituted flavonoid derivatives were synthesized and their anticholinesterase, anti-beta-amyloid (Aβ) aggregation and... 
Biochemistry, general | Biomedicine | Synthetic chemistry | Alzheimer’s disease | Pharmacology/Toxicology | Flavonoid | Cell Biology
Journal Article
Synthetic Communications, ISSN 0039-7911, 03/2015, Volume 45, Issue 6, pp. 741 - 749
A series of coumarin-resveratrol hybrids, 3-arylcoumarin derivatives 3a-u, were synthesized through the intermolecular condensation reaction of various... 
solvent-free | salicylaldehyde | 3-Arylcoumarins | DABCO | soybean 15-lipoxygenase | soybean 15-lipoxy-genase | soybean15-lipoxy-genase
Journal Article
Journal of Chemical Sciences, ISSN 0974-3626, 09/2016, Volume 128, Issue 9, pp. 1445 - 1449
An approach for the construction of benzotriazinone-triazole system is described. The synthesis is based on diazonium chemistry and subsequent intramolecular... 
acetylcholinesterase | nanocatalyst | benzotriazinone | diazonium chemistry | triazole | Triazole | DESIGN | COPPER NANOPARTICLES | V-TRIAZOLES | ANALOGS | CLICK CHEMISTRY | CHEMISTRY, MULTIDISCIPLINARY | ISOCYANIDE INSERTION | INHIBITORS | DERIVATIVES | IN-SITU | Usage | Catalysts | Triazoles | Physiological aspects | Chemical properties | Research | Acetylcholinesterase
Journal Article
Journal Article
Croatica Chemica Acta, ISSN 0011-1643, 11/2013, Volume 86, Issue 3, pp. 245 - 251
In the current project we focused on the synthesis of 4-Substituted-2-p-tolylthiazole derivatives. Cytotoxicity of synthesized compounds were evaluated against... 
Tyrosine kinase | Cytotoxicity | Docking | Phenylthiazole | Breast cancer | Synthesis | synthesis | docking | tyrosine kinase | breast cancer | CHEMISTRY, MULTIDISCIPLINARY | phenylthiazole | cytotoxicity | Thiazoles | Cell lines | Cancer cells | Chemical properties | Chemical synthesis | Health aspects | Methods | Production processes | Cells
Journal Article
Journal Article