Works matching IS 13811991 AND DT 2019 AND VI 23 AND IP 3
Results: 20
Synthesis, spectral characterization, docking studies and biological activity of urea, thiourea, sulfonamide and carbamate derivatives of imatinib intermediate.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 723, doi. 10.1007/s11030-018-9906-4
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Ciprofloxacin-functionalized magnetic silica nanoparticles: as a reusable catalyst for the synthesis of 1H-chromeno[2,3-d]pyrimidine-5-carboxamides and imidazo[1,2-a]pyridines.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 739, doi. 10.1007/s11030-018-9907-3
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Hybrids of oxoisoaporphine–tetrahydroisoquinoline: novel multi-target inhibitors of inflammation and amyloid-β aggregation in Alzheimer's disease.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 709, doi. 10.1007/s11030-018-9905-5
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A highly efficient precatalytic system (XPhos-PdG2) for the Suzuki–Miyaura cross-coupling of 7-chloro-1H-pyrrolo[2,3-c]pyridine employing low catalyst loading.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 697, doi. 10.1007/s11030-018-9904-6
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Synthesis and biological evaluation of benzomorpholine derivatives as novel EZH2 inhibitors for anti-non-small cell lung cancer activity.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 681, doi. 10.1007/s11030-018-9903-7
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5-Amino-pyrazoles: potent reagents in organic and medicinal synthesis.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 751, doi. 10.1007/s11030-018-9902-8
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Synthesis of benzosuberone-tethered spirooxindoles: 1-3-dipolar cycloaddition of azomethine ylides and arylidene benzosuberones.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 669, doi. 10.1007/s11030-018-9901-9
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Diastereoselective synthesis of cyclohexadienes via tandem cyclization strategies.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 651, doi. 10.1007/s11030-018-9900-x
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- Article
Second generation of primaquine ureas and bis-ureas as potential antimycobacterial agents.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 657, doi. 10.1007/s11030-018-9899-z
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A green, catalyst-free synthesis of pyrazolopyranopyrimidines in polyethylene glycol as a biodegradable medium at ambient temperature.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 639, doi. 10.1007/s11030-018-9898-0
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Synthesis and anticholinesterase activity of novel non-hepatotoxic naphthyridine-11-amine derivatives.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 625, doi. 10.1007/s11030-018-9897-1
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Synthesis, crystal structure and antimicrobial activity of 2-((2-(4-(1H-1,2,4-triazol-1-yl)phenyl)quinazolin-4-yl)oxy)-N-phenylacetamide derivatives against phytopathogens.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 615, doi. 10.1007/s11030-018-9896-2
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- Article
1,1-Diaryl compounds as important bioactive module in pesticides.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 809, doi. 10.1007/s11030-018-9895-3
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Three-dimensional descriptors for aminergic GPCRs: dependence on docking conformation and crystal structure.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 603, doi. 10.1007/s11030-018-9894-4
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Ammonium chloride-catalyzed green multicomponent synthesis of dihydropyrazine and tetrahydrodiazepine derivatives "on water".
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- Molecular Diversity, 2019, v. 23, n. 3, p. 585, doi. 10.1007/s11030-018-9893-5
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- Article
Synthesis of (E)-2-amino-N′-benzylidenehexahydroquinoline-3-carbohydrazide.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 593, doi. 10.1007/s11030-018-9892-6
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Design and synthesis of novel 2-(6-thioxo-1,3,5-thiadiazinan-3-yl)-N′-phenylacethydrazide derivatives as potential fungicides.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 573, doi. 10.1007/s11030-018-9891-7
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- Article
BET bromodomain inhibitors: fragment-based in silico design using multi-target QSAR models.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 555, doi. 10.1007/s11030-018-9890-8
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In silico studies, synthesis and anticancer activity of novel diphenyl ether-based pyridine derivatives.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 541, doi. 10.1007/s11030-018-9889-1
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Synthesis and characterization of Ni(II) complex functionalized silica-based magnetic nanocatalyst and its application in C–N and C–C cross-coupling reactions.
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- Molecular Diversity, 2019, v. 23, n. 3, p. 527, doi. 10.1007/s11030-018-9888-2
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