Works by Moloney, Mark G.
Results: 30
Microwave assisted, one-pot synthesis of 5-nitro- 2-aryl substituted-1H-benzimidazole libraries: Screening in vitro for antimicrobial activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2009, v. 24, n. 5, p. 1095, doi. 10.1080/14756360802632716
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- Article
LEAD(IV) REAGENTS: AN UNDERESTIMATED CLASS OF REAGENTS IN SYNTHESIS?
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- Main Group Metal Chemistry, 2001, v. 24, n. 9, p. 653
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- Article
LEAD(IV) REAGENTS FOR THE OXIDATION OF ALCOHOLS TO ALDEHYDES.
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- Main Group Metal Chemistry, 1998, v. 21, n. 1, p. 51
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- Article
NOVEL LEAD(IV) REAGENTS FOR CARBON-CARBON BOND FORMATION.
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- Main Group Metal Chemistry, 1996, v. 19, n. 3, p. 133
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- Article
SOME NOVEL LEAD(IV) TETRACARBOXYLATES: REAGENTS FOR CARBON-CARBON BOND FORMATION.
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- Main Group Metal Chemistry, 1995, v. 18, n. 6, p. 295
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- Article
Electron Promotion by Surface Functional Groups of Single Wall Carbon Nanotubes to Overlying Metal Particles in a Fuel-Cell Catalyst.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 28, p. 6998, doi. 10.1002/anie.201201589
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- Article
Negative-ion electrospray mass spectrometric analysis of dicarboxylic acids.
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- Journal of Mass Spectrometry, 1999, v. 34, n. 1, p. 60, doi. 10.1002/(SICI)1096-9888(199901)34:1<60::AID-JMS764>3.0.CO;2-Q
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- Article
Sonoelectrochemically Enhanced Electrocatalytic Processes: The Pb(IV) Catalyzed Cleavage of 1,2- cis-Cyclopentanediol at Graphite and Glassy Carbon Electrodes.
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- Electroanalysis, 1998, v. 10, n. 17, p. 1188, doi. 10.1002/(SICI)1521-4109(199811)10:17<1188::AID-ELAN1188>3.0.CO;2-L
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- Article
A qualitative structure activity relationship (SAR) study of selected pyroglutamates.
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- Journal of the Bangladesh Academy of Sciences, 2024, v. 48, n. 2, p. 165, doi. 10.3329/jbas.v48i2.70546
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- Article
Stereoselectivity of thiazolidine, malonamides and bicyclic tetramates with isopropyl NH and SH protecting group.
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- Journal of the Bangladesh Academy of Sciences, 2023, v. 47, n. 2, p. 215, doi. 10.3329/jbas.v47i2.66977
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- Article
Chemoselective Formation and Reaction of Densely Functionalised Bicyclic Tetramic Acids and Their Biological Activity.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 47, p. 7055, doi. 10.1002/ejoc.201701393
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- Article
Chiral Bicyclic Tetramates as Non-Planar Templates for Chemical Library Synthesis.
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- Chemical Biology & Drug Design, 2013, v. 81, n. 5, p. 645, doi. 10.1111/cbdd.12110
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- Article
Novel Chiral Skeletons for Drug Discovery: Antibacterial Tetramic Acids.
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- Chemical Biology & Drug Design, 2011, v. 78, n. 2, p. 229, doi. 10.1111/j.1747-0285.2011.01133.x
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- Article
A Detailed Study of Antibacterial 3-Acyltetramic Acids and 3-Acylpiperidine-2,4-diones.
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- ChemMedChem, 2014, v. 9, n. 8, p. 1826, doi. 10.1002/cmdc.201402093
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- Article
Introduction to Strategies for Organic Synthesis. By Laurie S. Starkey.
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- ChemMedChem, 2013, v. 8, n. 1, p. 164, doi. 10.1002/cmdc.201200440
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- Article
Robust Sub‐5 Nanometer bis(Diarylcarbene)‐Based Thin Film for Molecular Electronics and Plasmonics.
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- Advanced Materials, 2023, v. 35, n. 36, p. 1, doi. 10.1002/adma.202303057
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- Article
Nematicidal Activity of 3-Acyltetramic Acid Analogues Against Pine Wood Nematode, Bursaphelenchus xylophilus.
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- Molecules, 2017, v. 22, n. 9, p. 1568, doi. 10.3390/molecules22091568
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- Article
Larvicidal and Nematicidal Activities of 3-Acylbarbituric Acid Analogues against Asian Tiger Mosquito, Aedes albopictus, and Pine Wood Nematode, Bursaphelenchus xylophilus.
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- Molecules, 2017, v. 22, n. 7, p. 1196, doi. 10.3390/molecules22071196
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- Article
Antibacterial Barbituric Acid Analogues Inspired from Natural 3-Acyltetramic Acids; Synthesis, Tautomerism and Structure and Physicochemical Property-Antibacterial Activity Relationships.
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- Molecules, 2015, v. 20, n. 3, p. 3582, doi. 10.3390/molecules20033582
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- Article
Antibacterial Drug Releasing Materials by Post-Polymerization Surface Modification.
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- Journal of Molecular & Engineering Materials, 2017, v. 5, n. 1, p. -1, doi. 10.1142/S2251237317400056
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- Article
Post-Polymerization Modification of Materials using Diaryldiazomethanes: Changes to Surface Macroscopic Properties.
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- Macromolecular Reaction Engineering, 2014, v. 8, n. 2, p. 170, doi. 10.1002/mren.201200088
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- Article
Electron Promotion by Surface Functional Groups of Single Wall Carbon Nanotubes to Overlying Metal Particles in a Fuel-Cell Catalyst.
- Published in:
- Angewandte Chemie, 2012, v. 124, n. 28, p. 7104, doi. 10.1002/ange.201201589
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- Publication type:
- Article
Chemical functionalization of polyethylene surfaces by plasma-assisted carbene insertion.
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- Journal of Macromolecular Science: Pure & Applied Chemistry, 2017, v. 54, n. 12, p. 938, doi. 10.1080/10601325.2017.1381924
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- Article
Convenient preparations of racemic and enantiopure methyl 6-oxopipecolate.
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- Synthetic Communications, 1996, v. 26, n. 4, p. 687, doi. 10.1080/00397919608086742
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- Article
Carbene modification and reversible crosslinking of silver nanoparticles for controlled antibacterial activity.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72043-1
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- Article
Preparation, Post‐Modification, and Antibacterial Application of Gelatin Electrospun Membranes.
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- Macromolecular Bioscience, 2018, v. 18, n. 8, p. 1, doi. 10.1002/mabi.201800093
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- Article
Simple Efficient Synthesis of Strongly Luminescent Polypyrene with Intrinsic Conductivity and High Carbon Yield by Chemical Oxidative Polymerization of Pyrene.
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- Chemistry - A European Journal, 2010, v. 16, n. 16, p. 4803, doi. 10.1002/chem.200902621
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- Article
Tricyclic Fused Lactams by Mukaiyama Cyclisation of Phthalimides and Evaluation of their Biological Activity.
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- Antibiotics (2079-6382), 2023, v. 12, n. 1, p. 9, doi. 10.3390/antibiotics12010009
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- Article
Fused-Ring Oxazolopyrrolopyridopyrimidine Systems with Gram-Negative Activity.
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- Antibiotics (2079-6382), 2017, v. 6, n. 1, p. 2, doi. 10.3390/antibiotics6010002
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- Article
(8R,10aS)-Methyl 2,4-diamino-8-(tert-butyl)-6-oxo-6,8,10,10atetrahydrooxazolo[3'',4'':1',5']-pyrrolo[3',4':5,6]pyrido[2,3-d]pyrimidine-10a-carboxylate.
- Published in:
- Molbank, 2015, v. 2015, n. 4, p. 1, doi. 10.3390/M875
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- Article