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Приказ резултата 101-105 од 105
Stereoselective synthesis of alpha-hydroxy-beta-amino acids: the chiral pool approach
(Serbian Chemical Soc, Belgrade, 2004)
A method for the stereoselective homologation of alpha-amino acids into syn-alpha-hydroxy-beta-amino acids is described. based on the conversion of stereoisomeric cyanohydrins into trans-oxazolines. The synthetic potential ...
Reactions of alpha-4(20)-epoxy-5-O-mesyltriacetyltaxicine I induced by BF3 center dot Et2O/Bu4NBr
(Serbian Chemical Soc, Belgrade, 2006)
The reaction of alpha-4(20)-epoxy-5-O-mesyltriacetyltaxicin I (2) with (BF3Et2O)-Et-./Bu4NBr can give rise to 4 different products. Each of these products can be obtained selectively, under the appropriate reaction conditions.
The role of the thiol group in protein modification with methylglyoxal / Uloga tiolne grupe u modifikaciji proteina sa metilglioksalom
(Serbian Chemical Soc, Belgrade, 2009)
Methylglyoxal is a highly reactive a-oxoaldehyde with elevated production in hyperglycemia. It reacts with nucleophilic Lys and Arg side-chains and N-terminal amino groups causing protein modification. In the present study, ...
Synthesis, NMR, DFT and antimicrobial studies of Zn(II) complexes with N-benzyloxycarbonyl-S-alanine / Sinteza, NMR i DFT proračunavanja i ispitivanje antimikrobne aktivnosti Zn(II) kompleksa sa N-benziloksikarbonil-S-alaninom
(Serbian Chemical Soc, Belgrade, 2008)
In this study, the first complexes of Zn(II) with the N-benzyloxycarbonyl-S-alaninato ligand (N-Boc-S-ala) were synthesized. The new complexes were characterized by elemental analysis, conductometric measurements, IR. ...
The influence of dispersive interactions on the binding affinities of ligands with an arylpiperazine moiety to the dopamine D2 receptor / Uticaj disperzivnih interakcija na afinitet vezivanja liganada sa arilpiperazinskom funkcijom za dopaminski D2 receptor
(Serbian Chemical Soc, Belgrade, 2009)
Several isosteric 1,3-dihydro-5-[2-(4-aryl-l-piperazinyl)ethyl]-2H-benzinlidazole-2-thiones were used to investigate the interactions of different ligands with the binding site of the D2 receptor. Due to limitations of the ...