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One-pot five-component high diastereoselective synthesis of polysubstituted 2-piperidinones from aromatic aldehydes, nitriles, dialkyl malonates and ammonium acetate.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1327, doi. 10.1007/s11030-019-09997-6
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Diverse coordination of aroylhydrazones toward iron(III) in solid state and in solution: spectrometric, spectroscopic and computational study.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1253, doi. 10.1007/s11030-019-09989-6
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Conformational dynamics of α-conotoxin PnIB in complex solvent systems.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1291, doi. 10.1007/s11030-019-09993-w
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Cascade process for direct synthesis of indeno[1,2-b]furans and indeno[1,2-b]pyrroles from diketene and ninhydrin.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1313, doi. 10.1007/s11030-019-09996-7
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Intramolecular oxidative cyclization of N-(2,2,2-trifluoro-1-(phenylimino)ethyl)benzimidamide.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1301, doi. 10.1007/s11030-019-09995-8
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Efficient and environmentally sustainable domino protocol for the synthesis of diversified spiroheterocycles with privileged heterocyclic substructures using bio-organic catalyst in aqueous medium.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1355, doi. 10.1007/s11030-019-09999-4
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Estrone derived 2-naphthol analogue in the diastereoselective one-pot Betti-condensation.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1343, doi. 10.1007/s11030-019-09998-5
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Synthesis and in vitro anti-Toxoplasma gondii activity of a new series of aryloxyacetophenone thiosemicarbazones.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1223, doi. 10.1007/s11030-019-09986-9
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In silico prediction of drug-induced developmental toxicity by using machine learning approaches.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1281, doi. 10.1007/s11030-019-09991-y
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Design, synthesis, in silico and in vitro evaluation of novel diphenyl ether derivatives as potential antitubercular agents.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1265, doi. 10.1007/s11030-019-09990-z
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Synthesis and pharmacological properties of polysubstituted 2-amino-4H-pyran-3-carbonitrile derivatives.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1385, doi. 10.1007/s11030-019-09994-9
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One-pot synthesis of substituted pyrrole–imidazole derivatives with anticancer activity.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1177, doi. 10.1007/s11030-019-09982-z
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Coumarins: antifungal effectiveness and future therapeutic scope.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1367, doi. 10.1007/s11030-019-09992-x
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A green method for the synthesis of pyrrole derivatives using arylglyoxals, 1,3-diketones and enaminoketones in water or water–ethanol mixture as solvent.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1205, doi. 10.1007/s11030-019-09984-x
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Synthesis and biological evaluation of 1,2,4-triazolidine-3-thiones as potent acetylcholinesterase inhibitors: in vitro and in silico analysis through kinetics, chemoinformatics and computational approaches.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1185, doi. 10.1007/s11030-019-09983-y
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Facile synthesis of novel amino acid-like building blocks by N-alkylation of heterocyclic carboxylates with N-Boc-3-iodoazetidine.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1235, doi. 10.1007/s11030-019-09987-8
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Synthesis and molecular docking studies of novel pyrimidine derivatives as potential antibacterial agents.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1165, doi. 10.1007/s11030-019-10019-8
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Antiproliferative activity and apoptosis induction, of organo-antimony(III)–copper(I) conjugates, against human breast cancer cells.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1095, doi. 10.1007/s11030-019-10014-z
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Synthesis of spirooxindolocarbamates based on Betti reaction: antibacterial, antifungal and antioxidant activities.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1139, doi. 10.1007/s11030-019-10017-w
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Polythiophene‐functionalized magnetic carbon nanotube-supported copper(I) complex: a novel and retrievable heterogeneous catalyst for the "Phosphine- and Palladium-Free" Suzuki–Miyaura cross-coupling reaction.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1125, doi. 10.1007/s11030-019-10016-x
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Discovery and evaluation of inhibitory activity and mechanism of arylcoumarin derivatives on Theileria annulata enolase by in vitro and molecular docking studies.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1149, doi. 10.1007/s11030-019-10018-9
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Modeling antimalarial and antihuman African trypanosomiasis compounds: a ligand- and structure-based approaches.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1107, doi. 10.1007/s11030-019-10015-y
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Development of classification models for identification of important structural features of isoform-selective histone deacetylase inhibitors (class I).
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1077, doi. 10.1007/s11030-019-10013-0
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Design and synthesis of novel spirooxindole–indenoquinoxaline derivatives as novel tryptophanyl-tRNA synthetase inhibitors.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1043, doi. 10.1007/s11030-019-10011-2
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Synthesis and biological evaluation of 2-phenyl-4-aminoquinolines as potential antifungal agents.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1065, doi. 10.1007/s11030-019-10012-1
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Synthesis and anthelmintic activity of benzopyrano[2,3-c]pyrazol-4(2H)-one derivatives.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1025, doi. 10.1007/s11030-019-10010-3
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Synthesis of new pyrimidine-containing compounds: 5-(2-(alkylamino)-1,3-dioxo-2,3-dihydro-1H-inden-2-yl)-6-hydroxypyrimidine-2,4(1H,3H)-dione derivatives.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1015, doi. 10.1007/s11030-019-10009-w
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Design and synthesis of benzodiazepine-1,2,3-triazole hybrid derivatives as selective butyrylcholinesterase inhibitors.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 997, doi. 10.1007/s11030-019-10008-x
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Immobilization of platinum nanoparticles on the functionalized chitosan particles: an efficient catalyst for reduction of nitro compounds and tandem reductive Ugi reactions.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 985, doi. 10.1007/s11030-019-10007-y
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Design, synthesis, molecular docking and in vitro evaluation of benzothiazole derivatives as 11β-hydroxysteroid dehydrogenase type 1 inhibitors.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 1, doi. 10.1007/s11030-019-10006-z
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Structure elaboration of isoniazid: synthesis, in silico molecular docking and antimycobacterial activity of isoniazid–pyrimidine conjugates.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 949, doi. 10.1007/s11030-019-10004-1
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Insight into structural requirements of ACE inhibitory dipeptides: QSAR and molecular docking studies.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 957, doi. 10.1007/s11030-019-10005-0
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Comprehensive bioinformatics study reveals targets and molecular mechanism of hesperetin in overcoming breast cancer chemoresistance.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 933, doi. 10.1007/s11030-019-10003-2
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When global and local molecular descriptors are more than the sum of its parts: Simple, But Not Simpler?
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- Molecular Diversity, 2020, v. 24, n. 4, p. 913, doi. 10.1007/s11030-019-10002-3
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Green synthesis and characterization of novel 1,2,4,5-tetrasubstituted imidazole derivatives with eco-friendly red brick clay as efficacious catalyst.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 889, doi. 10.1007/s11030-019-10000-5
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Pd(NHC)(cinnamyl)Cl-catalyzed Suzuki cross-coupling reaction of aryl sulfonates with arylboronic acids.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 903, doi. 10.1007/s11030-019-10001-4
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