Ryszard Ostaszewski
Ryszard Ostaszewski
Institute of Organic Chemistry
Verified email at icho.edu.pl
Title
Cited by
Cited by
Year
TMAO: A small molecule of great expectations
M Ufnal, A Zadlo, R Ostaszewski
Nutrition 31 (11-12), 1317-1323, 2015
1522015
A tandem Petasis–Ugi multi component condensation reaction: solution phase synthesis of six dimensional libraries
DE Portlock, R Ostaszewski, D Naskar, L West
Tetrahedron letters 44 (3), 603-605, 2003
742003
KINETICALLY STABLE COMPLEXES OF ALKALI CATIONS WITH CALIXSPHERANDS - AN EVALUATION OF SHIELDING
WII BAKKER, M HAAS, C KHOOBEATTIE, R OSTASZEWSKI
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 116 (1), 123-133, 1994
601994
CALIX (AZA-)CROWNS AS POTENTIAL IONOPHORES FOR DIVALENT AND TRIVALENT CATIONS
R OSTASZEWSKI, TW STEVENS, W VERBOOM
RECUEIL DES TRAVAUX CHIMIQUES DES PAYS-BAS-JOURNAL OF THE ROYAL NETHERLANDS …, 1991
601991
Model studies on the first enzyme-catalyzed Ugi reaction
S Kłossowski, B Wiraszka, S Berłożecki, R Ostaszewski
Organic Letters 15 (3), 566-569, 2013
562013
Solid-phase synthesis of five-dimensional libraries via a tandem Petasis–Ugi multi-component condensation reaction
DE Portlock, D Naskar, L West, R Ostaszewski, JJ Chen
Tetrahedron letters 44 (27), 5121-5124, 2003
562003
Intracolonic hydrogen sulfide lowers blood pressure in rats
L Tomasova, L Dobrowolski, H Jurkowska, M Wróbel, T Huc, K Ondrias, ...
Nitric Oxide 60, 50-58, 2016
512016
Enzymatic desymmetrization of 3-arylglutaric acid anhydrides
A Fryszkowska, M Komar, D Koszelewski, R Ostaszewski
Tetrahedron: Asymmetry 16 (14), 2475-2485, 2005
472005
Studies of the synthesis of all stereoisomers of MG-132 proteasome inhibitors in the tumor targeting approach
M Mroczkiewicz, K Winkler, D Nowis, G Placha, J Golab, R Ostaszewski
Journal of medicinal chemistry 53 (4), 1509-1518, 2010
382010
Solvent‐free Passerini reactions
D Koszelewski, W Szymanski, J Krysiak, R Ostaszewski
Synthetic Communications 38 (7), 1120-1127, 2008
372008
Dimeric peroxiredoxins are druggable targets in human Burkitt lymphoma
A Trzeciecka, S Klossowski, M Bajor, R Zagozdzon, P Gaj, A Muchowicz, ...
Oncotarget 7 (2), 1717, 2016
362016
Studies toward novel peptidomimetic inhibitors of thioredoxin–thioredoxin reductase system
S Kłossowski, A Muchowicz, M Firczuk, M Świech, A Redzej, J Golab, ...
Journal of medicinal chemistry 55 (1), 55-67, 2012
362012
Soft and dispersed interface-rich aqueous systems that promote and guide chemical reactions
S Serrano-Luginbühl, K Ruiz-Mirazo, R Ostaszewski, F Gallou, P Walde
Nature reviews chemistry 2 (10), 306-327, 2018
322018
α-Amino acids as acid components in the Passerini reaction: influence of N-protection on the yield and stereoselectivity
S Berłożecki, W Szymanski, R Ostaszewski
Tetrahedron 64 (41), 9780-9783, 2008
312008
Studies on the application of the Passerini reaction and enzymatic procedures to the synthesis of tripeptide mimetics
W Szymanski, M Zwolinska, R Ostaszewski
Tetrahedron 63 (32), 7647-7653, 2007
312007
Multicomponent diversity and enzymatic enantioselectivity as a route towards both enantiomers of α-amino acids—a model study
W Szymanski, R Ostaszewski
Tetrahedron: Asymmetry 17 (18), 2667-2671, 2006
312006
Adenanthin targets proteins involved in the regulation of disulphide bonds
A Muchowicz, M Firczuk, J Chlebowska, D Nowis, J Stachura, ...
Biochemical pharmacology 89 (2), 210-216, 2014
302014
A new and general method for the synthesis of tripeptide aldehydes based on the multi-component Ugi reaction
M Mroczkiewicz, R Ostaszewski
Tetrahedron 65 (20), 4025-4034, 2009
302009
Efficient Passerini reactions in an aqueous vesicle system
D Paprocki, D Koszelewski, P Walde, R Ostaszewski
RSC advances 5 (124), 102828-102835, 2015
252015
Studies on enzymatic synthesis of chiral non-racemic 3-arylglutaric acid monoesters
A Fryszkowska, M Komar, D Koszelewski, R Ostaszewski
Tetrahedron: Asymmetry 17 (6), 961-966, 2006
252006
The system can't perform the operation now. Try again later.
Articles 1–20