Zainteresowania

• general chemistry
• nmr
• analytical chemistry
• molecules
• amadori products
• glycation
• solid phase synthesis
• solid phase peptide synthesis
• mass spectrometry
• peptides and proteins

Dyscyplina naukowa

• nauki chemiczne

Najnowsze publikacje

• Intramolecularly stapled amphipathic peptides via a boron–sugar interaction.
• Breaking Global Diatropic Current to Tame Diradicaloid Character: Thiele's Hydrocarbon Under Macrocyclic Constraints
• Stapling of leu-enkephalin analogs with bifunctional reagents for prolonged analgesic activity
• B,N-doped PAHs from tridentate ‘Defects’ – a bottom-up convergent approach for π-extended systems.
• Microwave-assisted solid-phase synthesis of lactosylated peptides for food analytical application
• Edge decoration of anthracene switches global diatropic current that controls the acene reactivity
• High-Temperature, Solid-Phase Reaction of α-Amino Groups in Peptides with Lactose and Glucose: An Alternative Mechanism Leading to an α-Ketoacyl Derivative
• Peptide Stapling with Boronate Esters‐ A Reversible Folding of (Artificial) Peptide Chain to α‐Helix
• Reductive dimerization of macrocycles activated by BBr₃.
• Analysis of fragmentation pathways of peptide modified with quaternary ammonium and phosphonium group as ionization enhancers
• Selenium in Peptide Chemistry
• An optimised di-boronate-ChemMatrix affinity chromatography to trap deoxyfructosylated peptides as biomarkers of glycation.
• Isolation, characterization, anti-MRSA evaluation, and in-silico multi-target anti-microbial validations of actinomycin X₂ and actinomycin D produced by novel Streptomyces smyrnaeus UKAQ_23.
• Multi‐cation coordination in porphyrinoids.
• Attempting to synthesize lasso peptides using high pressure.
• Isobaric duplex based on a combination of ¹⁶O/¹⁸O enzymatic exchange and labeling with pyrylium salts.
• Lossen rearrangement of p-toluenesulfonates of N-oxyimides in basic condition, theoretical study, and molecular docking.
• Selective ESI-MS detection of carbonyl containing compounds by aminooxyacetic acid immobilized on a resin.
• HPLC–free method of synthesis of isotopically labeled deoxyfructosylated peptides
• Solid-phase synthesis of peptides containing aminoadipic semialdehyde moiety and their cyclisations.