Teodozyj Kolasa
Publications by Year
Research Areas
Chemical Synthesis and Analysis, Synthesis and Biological Evaluation, Synthesis and Reactions of Organic Compounds, Crystallization and Solubility Studies, X-ray Diffraction in Crystallography
Most-Cited Works
- → Synthesis of 4,5-Diaryl-1H-pyrazole-3-ol Derivatives as Potential COX-2 Inhibitors(2004)91 cited
- → Reactions of .alpha.-hydroxy carbonyl compounds with azodicarboxylates and triphenylphosphine: synthesis of .alpha.-N-hydroxy amino acid derivatives(1987)74 cited
- → Structure−Activity Relationship of Triazafluorenone Derivatives as Potent and Selective mGluR1 Antagonists(2005)71 cited
- → Activators of soluble guanylate cyclase for the treatment of male erectile dysfunction(2002)62 cited
- → Synthesis of chiral zileuton, a potent and selective inhibitor of 5-lipoxygenase(1992)55 cited
- → Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A‐841720, a novel non‐competitive mGluR1 receptor antagonist(2006)50 cited
- → Activation of soluble guanylate cyclase causes relaxation of corpus cavernosum tissue: synergism of nitric oxide and YC-1(2002)49 cited
- → ABT-963 [2-(3,4-Difluoro-phenyl)-4-(3-hydroxy-3-methyl-butoxy)-5-(4-methanesulfonyl-phenyl)-2 H-pyridazin-3-one], A Highly Potent and Selective Disubstituted Pyridazinone Cyclooxgenase-2 Inhibitor(2004)45 cited
- → Preparation of (R)-(+)-N-[3-[5-[(4-Fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea (ABT-761), a second-generation 5-lipoxygenase inhibitor.(1995)44 cited
- → Quantitative determination of hydroxylamine(1974)44 cited