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Design, synthesis, and anti-inflammatory activity of novel 20-O-substituted camptothecin carbamate derivatives.
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 5/6, p. 304, doi. 10.1007/s10593-024-03338-8
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- Article
Pivotal Role of the Basic Character of Organic and Salt Catalysts in C−N Bond Forming Reactions of Amines with CO<sub>2</sub>.
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- Angewandte Chemie, 2020, v. 132, n. 3, p. 1014, doi. 10.1002/ange.201906942
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- Article
Rhodium-Catalyzed Diastereoselective Cyclization of Allenyl-Sulfonylcarbamates: A Stereodivergent Approach to 1,3-Aminoalcohol Derivatives.
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- Angewandte Chemie, 2016, v. 128, n. 50, p. 15798, doi. 10.1002/ange.201609366
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- Article
[Cu<sub>13</sub>{S<sub>2</sub>CN<sup> n</sup>Bu<sub>2</sub>}<sub>6</sub>(acetylide)<sub>4</sub>]<sup>+</sup>: A Two-Electron Superatom.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14924, doi. 10.1002/ange.201608609
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- Article
Optimization of the regioselective synthesis of mixed cellulose 3,5-dimethylphenyl and α-phenylethyl carbamate selectors as separation phases for chiral HPLC.
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- Cellulose, 2023, v. 30, n. 4, p. 2337, doi. 10.1007/s10570-022-05007-5
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- Article
Immobilization of a cellulose carbamate-type chiral selector onto silica gel by alkyne-azide click chemistry for the preparation of chiral stationary chromatography phases.
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- Cellulose, 2023, v. 30, n. 2, p. 915, doi. 10.1007/s10570-022-04932-9
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- Article
Exogenous Flupirtine as Potential Treatment for CLN3 Disease.
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- Cells (2073-4409), 2020, v. 9, n. 8, p. 1872, doi. 10.3390/cells9081872
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- Article
Acute Rat and Mouse Oral Toxicity Determination of Anticholinesterase Inhibitor Carbamate Pesticides: A QSTR Approach.
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- Molecular Informatics, 2019, v. 38, n. 8/9, p. 1, doi. 10.1002/minf.201800151
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- Article
Structural, stability and relaxation features of lanthanide‐complexes designed for multimodal imaging detection of enzyme activities.
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- European Journal of Inorganic Chemistry, 2024, v. 27, n. 14, p. 1, doi. 10.1002/ejic.202300784
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- Article
Dual‐protected amino acid derivatives as new antitubercular agents.
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- Chemical Biology & Drug Design, 2018, v. 92, n. 2, p. 1576, doi. 10.1111/cbdd.13315
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- Article
Structure-based approaches for the design of benzimidazole-2-carbamate derivatives as tubulin polymerization inhibitors.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 1, p. 40, doi. 10.1111/cbdd.12926
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- Article
PXD101 analogs with L-phenylglycine-containing branched cap as histone deacetylase inhibitors.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 4, p. 574, doi. 10.1111/cbdd.12787
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- Article
Design, Synthesis, and Biological Evaluation of Scutellarein Carbamate Derivatives as Potential Multifunctional Agents for the Treatment of Alzheimer's Disease.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 5, p. 1168, doi. 10.1111/cbdd.12580
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- Article
Bispidines for Dual Imaging.
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- Chemistry - A European Journal, 2014, v. 20, n. 51, p. 17011, doi. 10.1002/chem.201404086
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- Article
Synthesis and investigation of new cholesteryl carbamate-based liquid crystals.
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- Journal of Materials Science: Materials in Electronics, 2022, v. 33, n. 15, p. 12224, doi. 10.1007/s10854-022-08182-0
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- Article
Pre-treatments of pre-consumer cotton-based textile waste for production of textile fibres in the cold NaOH(aq) and cellulose carbamate processes.
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- Cellulose, 2021, v. 28, n. 6, p. 3869, doi. 10.1007/s10570-021-03753-6
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- Article
Production of cellulose carbamate using urea-based deep eutectic solvents.
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- Cellulose, 2018, v. 25, n. 1, p. 195, doi. 10.1007/s10570-017-1465-9
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- Article
Synthesis of poly(phenylacetylene)s containing chiral phenylethyl carbamate residues as coated‐type CSPs with high solvent tolerability.
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- Chirality, 2020, v. 32, n. 5, p. 547, doi. 10.1002/chir.23199
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- Article
QSTR Modeling to Find Relevant DFT Descriptors Related to the Toxicity of Carbamates.
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- Molecules, 2022, v. 27, n. 17, p. 5530, doi. 10.3390/molecules27175530
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- Article
Anti-Proliferative and Cytoprotective Activity of Aryl Carbamate and Aryl Urea Derivatives with Alkyl Groups and Chlorine as Substituents.
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- Molecules, 2022, v. 27, n. 11, p. 3616, doi. 10.3390/molecules27113616
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- Article
Synthesis of Polyanionic Cellulose Carbamates by Homogeneous Aminolysis in an Ionic Liquid/DMF Medium.
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- Molecules, 2022, v. 27, n. 4, p. 1384, doi. 10.3390/molecules27041384
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- Article
Hf(OTf) 4 -Catalyzed Three-Component Synthesis of N -Carbamate-Protected β-Amino Ketones.
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- Molecules, 2022, v. 27, n. 3, p. 1122, doi. 10.3390/molecules27031122
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- Article
Transition Metal-Free Synthesis of Halobenzo[ b ]furans from O -Aryl Carbamates via o -Lithiation Reactions †.
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- Molecules, 2022, v. 27, n. 2, p. 525, doi. 10.3390/molecules27020525
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- Article
Assessment of the Activity of Decoquinate and Its Quinoline- O -Carbamate Derivatives against Toxoplasma gondii In Vitro and in Pregnant Mice Infected with T. gondii Oocysts.
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- Molecules, 2021, v. 26, n. 21, p. 6393, doi. 10.3390/molecules26216393
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- Article
Targeting Monoacylglycerol Lipase in Pursuit of Therapies for Neurological and Neurodegenerative Diseases.
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- Molecules, 2021, v. 26, n. 18, p. 5668, doi. 10.3390/molecules26185668
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- Article
Metronidazole and Secnidazole Carbamates: Synthesis, Antiprotozoal Activity, and Molecular Dynamics Studies.
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- Molecules, 2020, v. 25, n. 4, p. 793, doi. 10.3390/molecules25040793
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- Article
Exploring New Structural Features of the 18β-Glycyrrhetinic Acid Scaffold for the Inhibition of Anaplastic Lymphoma Kinase.
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- Molecules, 2019, v. 24, n. 19, p. 3631, doi. 10.3390/molecules24193631
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- Article
Synthesis of Some New Thieno[2,3-b]pyridines, Pyrimidino[4',5':4,5]thieno[2,3-b]pyridine and Pyridines Incorporating 5-Bromobenzofuran-2-yl Moiety.
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- Molecules, 2015, v. 20, n. 1, p. 822, doi. 10.3390/molecules20010822
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- Article
New Water-Soluble Carbamate Ester Derivatives of Resveratrol.
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- Molecules, 2014, v. 19, n. 10, p. 15900, doi. 10.3390/molecules191015900
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Metabolomic and proteomic insights into carbaryl catabolism by Burkholderia sp. C3 and degradation of ten N-methylcarbamates.
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- Biodegradation, 2013, v. 24, n. 6, p. 795, doi. 10.1007/s10532-013-9629-2
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- Article
Direct Access to Carbamates through Palladium‐Catalyzed Carbonylation of Nitroarenes and Siloxanes.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 6, p. 1, doi. 10.1002/ajoc.202400078
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- Article
Antiproliferative Activities and SwissADME Predictions of Physicochemical Properties of Carbonyl Group‐Modified Rotenone Analogues.
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- ChemistryOpen, 2024, v. 13, n. 1, p. 1, doi. 10.1002/open.202300087
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- Article
Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane.
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- Journal of the Chinese Chemical Society, 2020, v. 67, n. 7, p. 1289, doi. 10.1002/jccs.201900434
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- Article
Microwave‐Assisted 1,3‐Dioxa‐[3,3]‐Sigmatropic Rearrangement of Substituted Allylic Carbamates: Application to the Synthesis of Novel 1,3‐Oxazine‐2,4‐dione Derivatives.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 1, p. 1, doi. 10.1002/ejoc.202101100
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- Article
Recent Advances in the Synthesis of Sulfonylureas.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 8, p. 1201, doi. 10.1002/ejoc.202001437
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- Article
Regio‐ and Enantioselective α,γ‐Dialkylation of α,β‐Unsaturated Aldehydes Through Cascade Organocatalysis.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 18, p. 2720, doi. 10.1002/ejoc.202000245
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- Article
Synthesis of Carbamates from Alkyl Bromides and Secondary Amines Using Silver Carbonate.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 3, p. 378, doi. 10.1002/ejoc.201901649
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- Article
Asymmetric Allylic Amination of Morita–Baylis–Hillman Carbonates with Silylated tert-Butylhydroxycarbamate Derivatives.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 14, p. 1926, doi. 10.1002/ejoc.201700222
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- Article
A Dinuclear Copper(II) Complex Electrochemically Obtained via the Endogenous Hydroxylation of a Carbamate Schiff Base Ligand: Synthesis, Structure and Catalase Activity.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 4, p. 2154, doi. 10.3390/ijms25042154
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- Article
Polyurethanes Modified by Ionic Liquids and Their Applications.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 14, p. 11627, doi. 10.3390/ijms241411627
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- Article
Lycorine Carbamate Derivatives for Reversing P-glycoprotein-Mediated Multidrug Resistance in Human Colon Adenocarcinoma Cells.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2061, doi. 10.3390/ijms24032061
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- Article
Synthesis of Four Steroidal Carbamates with Antitumor Activity against Mouse Colon Carcinoma CT26WT Cells: In Vitro and In Silico Evidence.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 15, p. 8775, doi. 10.3390/ijms23158775
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- Article
Synthesis and Enantioselective Pharmacokinetic/Pharmacodynamic Analysis of New CNS-Active Sulfamoylphenyl Carbamate Derivatives.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3361, doi. 10.3390/ijms22073361
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- Article
Synthesis of New Steroidal Carbamates with Plant-Growth-Promoting Activity: Theoretical and Experimental Evidence.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 5, p. 2330, doi. 10.3390/ijms22052330
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- Article
SAR-mediated Similarity Assessment of the Property Profile for New, Silicon-Based AChE/BChE Inhibitors.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 21, p. 5385, doi. 10.3390/ijms20215385
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Isolation and Cytotoxicity Evaluation of the Chemical Constituents from Cephalantheropsis gracilis.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 2, p. 3980, doi. 10.3390/ijms16023980
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- Article
tert -Butyl Bis(4′-(Hexyloxy)-[1,1′-biphenyl]-4-yl)carbamate.
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- Molbank, 2021, v. 2021, n. 3, p. M1247, doi. 10.3390/M1247
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- Article
(3-Ammonio-2,2-dimethyl-propyl)carbamate Dihydrate.
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- Molbank, 2018, v. 2018, n. 3, p. m1015, doi. 10.3390/M1015
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Carbamate derivatives of colchicine show potent activity towards primary acute lymphoblastic leukemia and primary breast cancer cells—in vitro and ex vivo study.
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- Journal of Biochemical & Molecular Toxicology, 2020, v. 34, n. 6, p. 1, doi. 10.1002/jbt.22487
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- Article
Colour changes in pulses fumigated with different metal phosphide formulations.
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- Julius-Kühn-Archiv, 2018, n. 463, p. 961, doi. 10.5073/jka.2018.463.208
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- Article