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Pavla Bojarová

Researcher at Academy of Sciences of the Czech Republic

Publications -  83
Citations -  1924

Pavla Bojarová is an academic researcher from Academy of Sciences of the Czech Republic. The author has contributed to research in topics: Chemistry & Glycosylation. The author has an hindex of 23, co-authored 67 publications receiving 1529 citations. Previous affiliations of Pavla Bojarová include Schiller International University & University of Melbourne.

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Selectively Deoxyfluorinated N-Acetyllactosamine Analogues as 19F NMR Probes to Study Carbohydrate-Galectin Interactions.

TL;DR: In this article, a complete series of six mono-deoxyfluorinated analogues of N-Acetyllactosamine (Galβ1-4GlcNAc, LacNAc) was synthesized, in which each hydroxyl has been selectively replaced by fluorine while the anomeric position has been protected as methyl β-glycoside.
OtherDOI

Glycosidases in synthesis

TL;DR: In recent decades, there has been a boom in carbohydrate chemistry, evoked by the increasing need for new carbohydrate materials and by the dynamic development of glycomics as mentioned in this paper, however, the tedious protection, activation, and dep...
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Recent trends in the treatment of cyanide-containing effluents: Comparison of different approaches

TL;DR: A review of recent advances in this research area can be found in this paper , where a general overview of innovative methods of different types (oxidation, flocculation, adsorption, electro(dia)lysis, photocatalysis, bioassimilation, biocatalysis).
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Glycosidases in Carbohydrate Synthesis: When Organic Chemistry Falls Short

TL;DR: In this paper, two approaches to glycosidase catalysis are presented: (i) the use of structurally modified substrates that carry various functional moieties in the molecule, and (ii) the design of mutant glyco-sidases void of hydrolytic activity.
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Discovery of human hexosaminidase inhibitors by in situ screening of a library of mono- and divalent pyrrolidine iminosugars.

TL;DR: In this article , two libraries of mono-and dimeric pyrrolidine iminosugars were synthesized by CuAAC and (thio)urea-bond-forming reactions from the respective azido/aminohexylpyrrolidine iminosugar precursors.