Name and surname:
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Mgr. Ambroz Almássy, PhD.
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Document type:
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Research/art/teacher profile of a person
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The name of the university:
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Comenius University Bratislava
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The seat of the university:
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Šafárikovo námestie 6, 818 06 Bratislava
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III.a - Occupation-position | III.b - Institution | III.c - Duration |
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Post-doc | Department of Physical Chemistry, University of Debrecen, Hungary | 2007-2008 |
Post-doc | Department of Inorganic Chemistry, University of Zaragoza and Department of Inorganic Chemistry, University of Burgos, Spain | 2008-2009 |
Post-doc | Department of Physical Chemistry, University of Debrecen, Hungary | 2009-2010 |
Assistant Professor | Department of Organic Chemistry, Comenius University, Bratislava | 2010-2024 |
V.1.a - Name of the profile course | V.1.b - Study programme | V.1.c - Degree | V.1.d - Field of study |
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Experimental Organic Chemistry 2 | Chemistry, Biochemistry | I. | Chemistry |
Organic Chemistry 2, seminar | Chemistry | I. | Chemistry |
Molecular Spectroscopy | Chemistry | I. | Chemistry |
I. | Chemistry |
V.5.a - Name of the course | V.5.b - Study programme | V.5.c - Degree | V.5.d - Field of study |
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Intruduction to Bioorganic Chemistry | Biology, Medicinal Biology | I. | Biology |
Seminar on Organic Chemistry | Biological Chemistry | I. | Chemistry |
Natural Compounds | Biology, medicinal biology, chemistry, biochemistry | I. | Chemistry, biochemistry, biology |
Bioorganic Chemistry 1 | Organic and bioorganic chemistry | II. | chemistry |
Chemistry of Natural Products | Organic and Bioorganic Chemistry | II. | Chemistry |
Organic Chemistry 2 | I. | Biological Chemistry |
Novel Sulfonated N-Heterocyclic Carbene Gold(I) Complexes: Homogeneous Gold Catalysis for the Hydration of Terminal Alkynes in Aqueous Media. A. Almassy, C. E. Nagy, A. C. Benyei, F. Joo, Organometallics 2010, 29, 2484-2490. https://doi.org/10.1021/om1001292
Ferrocene phosphane-carbene ligands in Cu-catalyzed enantioselective 1,4-additions of Grignard reagents to alpha,beta-unsaturated carbonyl compounds. Z. Csizmadiova, M. Meciarova, A. Almassy, B. Horvath, R. Sebesta, J. Organomet. Chem. 2013, 737, 47-52. https://doi.org/10.1016/j.jorganchem.2013.03.033
New [5]ferrocenophane diphosphine ligands for Pd-catalyzed allylic substitution. R. Sebesta, A. Almassy, I. Cisarova, S. Toma, Tetrahedron Asymmetry, 2006, 17, 2531-2537. https://doi.org/10.1016/j.tetasy.2006.09.011
Thiol-Free Synthesis of Oseltamivir and Its Analogues via Organocatalytic Michael Additions of Oxyacetaldehydes to 2-Acylaminonitroalkenes. J. Rehak, M. Hutka, A. Latika, H. Brath, A. Almassy, V. Hajzer, J. Durmis, S. Toma, R. Sebesta, Synthesis, 2012, 44, 15, 2424-2430. https://doi.org/10.1055/s-0031-1290396
Explanation of Different Regioselectivities in the ortho-Lithiation of Ferrocenyl(phenyl)methanamines. Almassy, A.; Skvorcova, A.; Horvath, B.; Bilcik, F.; Bariak, V.; Rakovsky, E.; Sebesta, R. Chem. Pap. 2013, 1, 111-116. https://doi.org/10.1002/ejoc.201201325
Unusual Chemistry in an Uncatalyzed Bromate-Aniline Oscillator: Ring-Contraction Oxidation of Aniline with Pulsative CO2 Production. I. Valent, M. Pribus, F. Novak, S. Plankova, J. Blasko, R. Kubinec, A. Almassy, J. Filo, I. Sigmundova, T. Sebechlebska, T. B. Lawson, Z. Noszticzius, J. Phys. Chem. A 2019, 123, 9669-9681. https://doi.org/10.1021/acs.jpca.9b07766
Assessing Basic Separatory Technique Skills in an Organic Experiment Based on an Incomplete Haloform Reaction. I. Kmentová, A. Almássy, L. Feriancová, M. Putala, J. Chem. Educ. 2020, 97, 4, 1139–1144. https://doi.org/10.1021/acs.jchemed.9b01015
Isomerization of Ferrocenyl Phosphinites to Phosphane-oxides and retro-Phospha-Brook Rearrangement. A. Almássy, A. Hejtmánková, D. Vargová, R. Šebesta, 2021, 941, 121801. https://doi.org/10.1016/j.jorganchem.2021.121801
Selectivity of N(2)-substituted oxotriazinoindole aldose reductase inhibitors is determined by the interaction pattern with Pro301-Arg312 loop of aldehyde reductase. L. Kováčiková, S. Gaikwad, K. Almášiová, A. Almássy, G. Addová, M. Májeková, G. Hanquet, V. Dobričić, A. Boháč, M. Štefek, Med Chem Res 2024, 33, 492–503. http://dx.doi.org/10.2139/ssrn.4382808
Organometallics 2010, 29, 2484: Li, F.; Wang, N. N.; Lu, L.; Zhu, G. J. Regioselective Hydration of Terminal Alkynes Catalyzed by a Neutral Gold(I) Complex [(IPr)AuCl] and One-Pot Synthesis of Optically Active Secondary Alcohols from Terminal Alkynes by the Combination of [(IPr)AuCl] and Cp*RhCl[(R,R)-TsDPEN]. Org. Chem. 2015, 80, 7, 3538-3546.
Organometallics 2010, 29, 2484: Levin, E.; Ivry, E.; Diesendruck, C. E.; Lemcoff, N. G. Water in N-Heterocyclic Carbene-Assisted Catalysis. Chem. Rev. 2015, 115, 11, 4607-4692.
Chem. - Eur. J. 2015, 21, 13445: Korb, M.; Lang, H. The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics. Chem. Soc. Rev. 2019, 48, 10, 2829.
Tetrahedron Asymmetry, 2006, 17, 2531: Ogasawara, M.; Arae, S.; Watanabe, S.; Nakajima, K.; Takahashi, T. Kinetic Resolution of Planar-Chiral Ferrocenylphosphine Derivatives by Molybdenum-Catalyzed Asymmetric Ring-Closing Metathesis and Their Application in Asymmetric Catalysis. ACS Catalysis 2016, 6, 2, 1308.
Synthesis 2012, 44, 12, 2424: Hayashi, Y. Time and Pot Economy in Total Synthesis. Acc. Chem. Res. 2021, 54, 6, 1385.
Synthesis of ferrocene derivatives via direct C-H activation; VEGA 1/0590/19
Development of novel type of drug candidates against life threatening health complications caused by diabetes mellitus; 2023-2025; APVV SK-FR-22-0017
In vitro estimation of pharmacokinetic properties and molecular modelling – an integrated approach to the development of more efficient ALR2 inhibitors as potential drugs to treat diabetic complications; 2022-2023; APVV SK-SRB-21-0047
Medicinal chemistry - an effective development of inhibitors of selected key biological targets connected with tumour progression; 2018-2021; VEGA1/0670/18
VII.a - Activity, position | VII.b - Name of the institution, board | VII.c - Duration |
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Member of Academic Senate | Faculty of Natural Sciences, Comenius University, Bratislava | 2014-2021 |
Member of the Organizing Committee | 50th International Chemistry Olympiad | 2017-2018 |