about
Synthesis and antibacterial activity of monocyclic 3-carboxamide tetramic acidsMicrowave assisted, one-pot synthesis of 5-nitro- 2-aryl substituted-1H-benzimidazole libraries: screening in vitro for antimicrobial activity.Excitatory amino acids.Novel chiral skeletons for drug discovery: antibacterial tetramic acids.Chiral bicyclic tetramates as non-planar templates for chemical library synthesis.Synthesis of 3-acyltetramates by side chain manipulation and their antibacterial activity.A detailed study of antibacterial 3-acyltetramic acids and 3-acylpiperidine-2,4-diones.Synthesis of mimics of pramanicin from pyroglutamic acid and their antibacterial activity.Equisetin, reutericyclin and streptolodygin as natural product lead structures for novel antibiotic libraries.The oxazolomycins: a structurally novel class of bioactive compounds.Larvicidal and Nematicidal Activities of 3-Acylbarbituric Acid Analogues against Asian Tiger Mosquito, Aedes albopictus, and Pine Wood Nematode, Bursaphelenchus xylophilus.Surface Characterization and in situ Protein Adsorption Studies on Carbene-Modified Polymers.Surface functional polymers by post-polymerization modification using diarylcarbenes: introduction, release and regeneration of hydrogen peroxide and bactericidal activity.Simple efficient synthesis of strongly luminescent polypyrene with intrinsic conductivity and high carbon yield by chemical oxidative polymerization of pyrene.Pyrrolidinones derived from (S)-pyroglutamic acid: penmacric acid and analogues.2,5-Disubstituted pyrrolidines: versatile regioselective and diastereoselective synthesis by enamine reduction and subsequent alkylation.Enantiopure bicyclic piperidinones: stereoselectivity in lactam enolate alkylations.Enantiopure bicyclic piperidinones: stereocontrolled conjugate additions leading to substituted piperidinones.On the antibiotic activity of oxazolomycin.Stereoselective synthesis of conformationally constrained omega-amino acid analogues from pyroglutamic acid.Structural investigations of a lead(IV) tetraacetate-pyridine complex.Chemical functionalization of diamond surfaces by reaction with diaryl carbenes.Uncatalysed diaryldiazo cyclopropanations on bicyclic lactams: access to annulated prolines.Biomimetic synthesis, antibacterial activity and structure-activity properties of the pyroglutamate core of oxazolomycin.Mimics of pramanicin derived from pyroglutamic acid and their antibacterial activity.Electron promotion by surface functional groups of single wall carbon nanotubes to overlying metal particles in a fuel-cell catalyst.Diastereoselective reduction of the tricarbonyl moiety in bicyclic tetramates giving pyroglutamates.Synthesis and bioactivity of fused- and spiro-β-lactone-lactam systems.A multicomponent coupling strategy suitable for the synthesis of the triene component of the oxazolomycin antibiotics.Oxazolomycins: natural product lead structures for novel antibacterials by click fragment conjugation.Rapid diastereocontrolled synthesis of 2,2,5-trisubstituted pyrrolidines.Excitatory amino acidstrans-2,5-Disubstituted pyrrolidines: Rapid stereocontrolled access from sulfones2,5-Disubstituted pyrrolidines: synthesis by enamine reduction and subsequent regioselective and diastereoselective alkylationsUltrasensitive Pb(II) potentiometric sensor based on copolyaniline nanoparticles in a plasticizer-free membrane with a long lifetimeSynthesis of and tautomerism in 3-acyltetramic acidsControl of chemoselectivity in Dieckmann ring closures leading to tetramic acidsSpirocyclic systems derived from pyroglutamic acidRapid synthesis of substituted pyrrolines and pyrrolidines by nucleophilic ring closure at activated oximesAntibacterial barbituric acid analogues inspired from natural 3-acyltetramic acids; synthesis, tautomerism and structure and physicochemical property-antibacterial activity relationships
P50
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P50
description
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researcher
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հետազոտող
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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Mark G. Moloney
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P106
P1153
7102209893
P21
P31
P496
0000-0002-4440-3632