Publications
- The unexpected rearrangement of salicylanilide esters of amino acids - an explanation of the mechanismPublication without faculty affiliation
- Rearrangement forms of salicylestersPublication without faculty affiliation
- Salicylanilide amino acid esters rearrangement leads to antimycobacterial active di- and triamidesPublication without faculty affiliation
- Salicylanilide rearrangement - mechanism presentationPublication without faculty affiliation
- Salicylanilide esters of N-protected amino acids as novel antimicrobial agents2009 | Central Library of Charles University, Faculty of Pharmacy in Hradec Králové
- New antituberculotics originated from salicylanilides with promising in vitro activity against atypical mycobacterial strains2009 | Central Library of Charles University, Faculty of Pharmacy in Hradec Králové
- Recent advances on isoniazide derivatives2008 | Central Library of Charles University, Faculty of Pharmacy in Hradec Králové
- Salicylanilide esterification: unexpected formation of novel seven-membered rings2006 | Faculty of Pharmacy in Hradec Králové
- Hydrazonoderivatives of some antituberculotics as prodrugs, their stability in water conditionPublication without faculty affiliation
- Hydrolytic degradation studies of hydrazonoformamide prodrugs of isoniazidPublication without faculty affiliation
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