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Journal Article
Tetrahedron: Asymmetry, ISSN 0957-4166, 11/2017, Volume 28, Issue 11, pp. 1445 - 1461
[Display omitted] Isoquinuclidines constitute the central structural nucleus of numerous biologically active natural products, for example, iboga alkaloids... 
XESTOCYCLAMINE-A | CATHARANTHINE | CHEMISTRY, ORGANIC | CHEMISTRY, PHYSICAL | BIOMIMETIC ALKALOID SYNTHESES | (+/-)-CATHARANTHINE | DAPHNIPHYLLUM ALKALOIDS | PHARMACOLOGICAL-PROPERTIES | CHEMISTRY, INORGANIC & NUCLEAR | Alkaloids | Synthesis | Drug discovery | Organic compounds
Journal Article
Chemistry & Biodiversity, ISSN 1612-1872, 08/2017, Volume 14, Issue 8, pp. e1700035 - n/a
Journal Article
Synthetic Communications, ISSN 0039-7911, 02/2018, Volume 48, Issue 4, pp. 462 - 472
In world, many people struggle with viral, parasitic, bacterial, cancer, and other diseases. Therefore, numerous chemists seek to develop less toxic, more... 
ionic liquid | alkaline phosphatase | Acridines | enzyme inhibitor | DABCO | ORGANIC-SYNTHESIS | DESIGN | MECHANISM | CHEMISTRY, ORGANIC | MIXTURES | GROWTH | GENES | DERIVATIVES
Journal Article
Journal Article
Journal of Heterocyclic Chemistry, ISSN 0022-152X, 01/2017, Volume 54, Issue 1, pp. 780 - 783
A small series of new 3,5‐dimethyl‐4‐(arylsulfanyl)pyrazoles have been synthesized in good to excellent yields by a grinding‐induced, sequential one‐pot... 
CHEMISTRY, ORGANIC
Journal Article
Molecules, ISSN 1420-3049, 08/2017, Volume 22, Issue 8, p. 1352
Sulfonamide derivatives serve as an important building blocks in the drug design discovery and development (4D) process. Ciprofloxacin-, sulfadiazine-and... 
Kinetic mechanism | Drug discovery | Sulfonamides | Molecular docking | Drug derivatives | Jack bean urease inhibition | DESIGN | jack bean urease inhibition | BIOCHEMISTRY & MOLECULAR BIOLOGY | LIBRARY | sulfonamides | SIMULATION | CHEMISTRY, MULTIDISCIPLINARY | kinetic mechanism | PROTEASE INHIBITORS | PREDICTION | IN-VITRO | molecular docking | drug discovery | CHEMISTRY | drug derivatives | BINDING | CARBONIC-ANHYDRASE INHIBITORS | HYBRIDS | Amantadine - chemical synthesis | Sulfonamides - chemistry | Fabaceae - chemistry | Free Radical Scavengers - chemistry | Structure-Activity Relationship | Urease - antagonists & inhibitors | Enzyme Inhibitors - chemical synthesis | Urease - chemistry | Ciprofloxacin - analogs & derivatives | Sulfadiazine - chemical synthesis | Amantadine - analogs & derivatives | Sulfonamides - chemical synthesis | Amantadine - chemistry | Enzyme Inhibitors - chemistry | Sulfadiazine - analogs & derivatives | Ciprofloxacin - chemistry | Free Radical Scavengers - chemical synthesis | Inhibitory Concentration 50 | Sulfadiazine - chemistry | Molecular Docking Simulation | Fabaceae - enzymology | Kinetics | Ciprofloxacin - chemical synthesis | Enzymes | Sulfadiazine | Amantadine | Ascorbic acid | Jack beans | Urease | Lead compounds | Derivatives | Drug development | Inhibitors | Vitamin C | Thiourea | Inhibition | Ciprofloxacin | Chemical synthesis
Journal Article
Synlett, ISSN 0936-5214, 06/2016, Volume 27, Issue 9, pp. 1371 - 1374
Abstract A simple single-step methodology was developed to synthesize 3,7-dialkyltetrahydro-1 H ,5 H -[1,2,4]triazolo[1,2-a][1,2,4]triazole-1,5-dithiones in... 
letter | 4]triazole-1 | thiosemicarbazide | triazolo | 2-a | CHEMISTRY, ORGANIC | 5-dithiones | DERIVATIVES | aliphatic aldehydes
Journal Article
Journal of Photochemistry & Photobiology, B: Biology, ISSN 1011-1344, 12/2018, Volume 189, pp. 104 - 118
Journal Article