Works matching DE "CARBOXAMIDES"
Results: 697
Symmetric Aromatic Amidoalkylations of Triphenylenes.
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- Chemistry - A European Journal, 2024, v. 30, n. 54, p. 1, doi. 10.1002/chem.202402348
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Cover Feature: Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction (Chem. Eur. J. 50/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 50, p. 1, doi. 10.1002/chem.202402175
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Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction.
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- Chemistry - A European Journal, 2024, v. 30, n. 50, p. 1, doi. 10.1002/chem.202402175
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Palladium‐Catalyzed C‐H Olefination of Imidazo[1,2a] pyridine Carboxamide in Aqueous Ethanol under Oxygen.
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- Chemistry - A European Journal, 2024, v. 30, n. 23, p. 1, doi. 10.1002/chem.202304239
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Palladium‐Catalyzed Regiodivergent C‐H Olefination of Imidazo[1,2a]pyridine Carboxamide and Unactivated Alkenes.
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- Chemistry - A European Journal, 2023, v. 29, n. 70, p. 1, doi. 10.1002/chem.202302759
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An Iodide‐Mediated Anodic Amide Coupling.
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- Chemistry - A European Journal, 2022, v. 28, n. 54, p. 1, doi. 10.1002/chem.202201768
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How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides.
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- Chemistry - A European Journal, 2022, v. 28, n. 31, p. 1, doi. 10.1002/chem.202200755
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Front Cover: How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides (Chem. Eur. J. 31/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 31, p. 1, doi. 10.1002/chem.202201308
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How the Chalcogen Atom Size Dictates the Hydrogen‐Bond Donor Capability of Carboxamides, Thioamides, and Selenoamides.
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- Chemistry - A European Journal, 2022, v. 28, n. 31, p. 1, doi. 10.1002/chem.202200755
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Bifunctional Iminophosphorane Catalyzed Amide Enolization for Enantioselective Cyclohexadienone Desymmetrization.
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- Angewandte Chemie, 2024, v. 136, n. 5, p. 1, doi. 10.1002/ange.202315401
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Interaction between Divalent Copper Fluoride and Carboxamide Group Enabling Stereoretentive Fluorination of Tertiary Alkyl Halides.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202301343
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Transition‐Metal‐Free Reductive Functionalization of Tertiary Carboxamides and Lactams for α‐Branched Amine Synthesis.
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- Angewandte Chemie, 2020, v. 132, n. 29, p. 12001, doi. 10.1002/ange.202004272
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Enantioselective Palladium‐Catalyzed Cross‐Coupling of α‐Bromo Carboxamides and Aryl Boronic Acids.
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- Angewandte Chemie, 2019, v. 131, n. 33, p. 11477, doi. 10.1002/ange.201905174
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Nickel‐Catalyzed 1,1‐Alkylboration of Electronically Unbiased Terminal Alkenes.
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- Angewandte Chemie, 2019, v. 131, n. 26, p. 8964, doi. 10.1002/ange.201903890
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Copper‐Catalyzed Remote C(sp<sup>3</sup>)−H Trifluoromethylation of Carboxamides and Sulfonamides.
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- Angewandte Chemie, 2019, v. 131, n. 8, p. 2532, doi. 10.1002/ange.201813425
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Diastereoselective Aza‐Mislow–Evans Rearrangement of N‐Acyl tert‐Butanesulfinamides into α‐Sulfenyloxy Carboxamides.
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- Angewandte Chemie, 2018, v. 130, n. 47, p. 15809, doi. 10.1002/ange.201809551
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Synthesis and Biological Activity of 2-amino-1-aryl-5-(3,3-dimethyl-2-oxobutylidene)-4-oxo-N-(thiazol-5-yl)-4,5-dihydro-1h-pyrrole-3-carboxamides.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 3, p. 198, doi. 10.1007/s11094-018-1790-9
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Using Bioisosteric Replacements to Enhance the Analgesic Properties of 4-Hydroxy-6,7-Dimethoxy-2-oxo-1,2-Dihydroquinoline-3-Carboxamides.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 6, p. 365, doi. 10.1007/s11094-016-1453-7
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Synthesis and Analgesic Activity of N,6-diaryl-4-methyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 4, p. 226, doi. 10.1007/s11094-016-1427-9
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Synthesis and Antifungal Activity Against Candida Albicans of 6-Aryl-3,4-Dimethyl- N-Phenyl-2-Oxo-1,2,3,6-Tetrahydropyrimidine-5-Carboxamides.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 8, p. 509, doi. 10.1007/s11094-015-1316-7
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Synthesis and Antimicrobial Activity of N-5-Diaryl-7-Methyl-3-OXO-2,3-Dihydro-5 H-[1,3]Thiazolo[3,2- a]Pyrimidine-6-Carboxamide Hydrochlorides.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 8, p. 512, doi. 10.1007/s11094-015-1317-6
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Synthesis and Antimicrobial Activity of N,N′,2-Triaryl-6-Hydroxy-6-Methyl-4-Oxocyclohexane-1,3-Dicarboxamides.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 4, p. 246, doi. 10.1007/s11094-015-1264-2
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Synthesis and Antibacterial Evaluation of Carboxamide Derivatives of Amino Acids.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 1, p. 29, doi. 10.1007/s11094-014-1040-8
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Synthesis and Antimicrobial Activity of N,6-Diaryl-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides.
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- Pharmaceutical Chemistry Journal, 2013, v. 46, n. 12, p. 720, doi. 10.1007/s11094-013-0877-6
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Synthesis and biological properties of new derivatives of 2-arylpyrrolidinecarbonitriles and pyrrolidinecarboxamides.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 6, p. 331, doi. 10.1007/s11094-012-0792-2
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Synthesis and antimicrobial activity of N,6-diaryl-4-methyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 2, p. 114, doi. 10.1007/s11094-012-0743-y
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Synthesis and biological activity of new pyranochromen-3-carboxamides.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 1, p. 10, doi. 10.1007/s11094-012-0725-0
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Redetermination and Density Functional Studies of N,N′-(Disulfanediyldibenzene-2,1-Diyl) Dipyridine-2-Carboxamide.
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- Journal of Structural Chemistry, 2018, v. 59, n. 8, p. 1797, doi. 10.1134/S0022476618080061
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Molecular and crystal structure of (1 R,5 S)-8-oxo-1,5,6,8-tetrahydro-2 H-1,5-methanopyrido[1,2- a][1,5]diazocine-3(4 H)-carboxamide and (1 R,5 S)-8-OXO-1,5,6,8-tetrahydro-2 H-1,5-methanopyrido[1,2- a][1,5]diazocine-3(4 H)-thiocarboxamide.
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- Journal of Structural Chemistry, 2015, v. 56, n. 1, p. 188, doi. 10.1134/S0022476615010278
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Synthesis and antitumor activities of 2-(piperidin-4-yl)-thiazole-4-carboxamides analogues of tubulysins.
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- Turkish Journal of Chemistry, 2019, v. 43, n. 2, p. 676, doi. 10.3906/kim-1810-69
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Synthesis and charact erizations of novel thiazolyl-thiadiazole derivatives as telomerase activators.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 3, p. 768, doi. 10.3906/kim-1711-92
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Synthesis and structural properties of N-3,4-(dichlorophenyl)-3-oxo-3-phenyl-2-(phenylcarbonyl)propanamide and its Cu(II) complex.
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- Turkish Journal of Chemistry, 2016, v. 40, n. 1, p. 76, doi. 10.3906/kim-1501-32
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Synthesis of 5-aryl-N-(trichloroacetyl)-1,3,4-oxadiazole-2-carboxamide via three-component reaction of trichloroacetyl isocyanate, (N-isocyanimino)triphenylphosphorane, and benzoic acid derivatives.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 4, p. 874, doi. 10.3906/kim-1501-43
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Synthesis and Insecticidal Activity of Novel Trifluoromethylbenzimidazole Linked N-Phenylamide Compounds.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 9, p. 6125, doi. 10.1080/10406638.2023.2273885
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Synthesis and Characterization of Some New Pyridine-Carboxamide Derivatives of Potential Biological Activities.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 9, p. 5927, doi. 10.1080/10406638.2023.2270762
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Design, synthesis, and biological evaluation of thiazole/thiadiazole carboxamide scaffold-based derivatives as potential c-Met kinase inhibitors for cancer treatment.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2247183
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Design, synthesis, biological evaluation and QSAR analysis of novel N-substituted benzimidazole derived carboxamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1327, doi. 10.1080/14756366.2022.2070910
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Charged pyridinium oximes with thiocarboxamide moiety are equally or less effective reactivators of organophosphate-inhibited cholinesterases compared to analogous carboxamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 760, doi. 10.1080/14756366.2022.2041628
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Pyridinium-2-carbaldoximes with quinolinium carboxamide moiety are simultaneous reactivators of acetylcholinesterase and butyrylcholinesterase inhibited by nerve agent surrogates.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 437, doi. 10.1080/14756366.2020.1869954
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Design, synthesis, and screening of ortho-amino thiophene carboxamide derivatives on hepatocellular carcinomaas VEGFR-2Inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 1472, doi. 10.1080/14756366.2018.1503654
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Synthesis, biological activity and multiscale molecular modeling studies for coumaryl-carboxamide derivatives as selective carbonic anhydrase IX inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 1042, doi. 10.1080/14756366.2017.1354857
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Subnanomolar indazole-5-carboxamide inhibitors of monoamine oxidase B (MAO-B) continued: indications of iron binding, experimental evidence for optimised solubility and brain penetration.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 960, doi. 10.1080/14756366.2017.1344980
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Lipid lowering activity of novel N -(benzoylphenyl)pyridine-3-carboxamide derivatives in Triton WR-1339-induced hyperlipidemic rats.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 138, doi. 10.1080/14756366.2016.1222581
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Design, synthesis and biological activity of 1H-indene-2-carboxamides as multi-targeted anti-Alzheimer agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 13, doi. 10.1080/14756366.2016.1186019
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Metal based drugs: design, synthesis and in-vitro antimicrobial screening of Co(II), Ni(II), Cu(II) and Zn(II) complexes with some new carboxamide derived compounds: crystal structures of N-[ethyl(propan-2-yl)carbamothioyl]thiophene-2-carboxamide and its copper(II) complex
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 4, p. 590, doi. 10.3109/14756366.2015.1050011
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Synthesis and in vitro pharmacological evaluation of N -[(1-benzyl-1,2,3-triazol-4-yl)methyl]-carboxamides on d -secoestrone scaffolds.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 4, p. 574, doi. 10.3109/14756366.2015.1050008
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Pharmacokinetic evaluation of C-3 modified 1,8-naphthyridine-3-carboxamide derivatives with potent anticancer activity: lead finding.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 5, p. 710, doi. 10.3109/14756366.2013.845817
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Metal-based carboxamide-derived compounds endowed with antibacterial and antifungal activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 4, p. 517, doi. 10.3109/14756366.2013.815178
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Synthesis and cytotoxicity studies of novel benzhydrylpiperazine carboxamide and thioamide derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 2, p. 205, doi. 10.3109/14756366.2013.765416
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Synthesis, characterization and antimicrobial activity of novel xanthene sulfonamide and carboxamide derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 5, p. 885, doi. 10.3109/14756366.2012.692087
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