F. Demeter

发表

Systematic Study of Regioselective Reductive Ring-Opening Reactions of 4,6-O-Halobenzylidene Acetals of Glucopyranosides.

Ilona Bereczki, A. Borbás, M. Csávás, 2021, The Journal of organic chemistry.

Synthesis of α-1,2- and α-1,3-linked di-rhamnolipids for biological studies.

Margaret Dah-Tsyr Chang, A. Borbás, Yuan-chuan Lee, 2020, Carbohydrate research.

Synthesis and Cell Growth Inhibitory Activity of Six Non‐glycosaminoglycan‐Type Heparin‐Analogue Trisaccharides

S. Bősze, A. Borbás, Lilla Horváth, 2021, ChemMedChem.

Short Synthesis of Idraparinux by Applying a 2-O -Methyl-4,6-O -arylmethylene Thioidoside as a 1,2-trans -α-Selective Glycosyl Donor

A. Borbás, M. Herczeg, F. Demeter, 2018, European Journal of Organic Chemistry.

Synthesis of Four Orthogonally Protected Rare l-Hexose Thioglycosides from d-Mannose by C-5 and C-4 Epimerization

Ilona Bereczki, A. Borbás, M. Herczeg, 2022, Molecules.

Rapid Synthesis of l -Idosyl Glycosyl Donors from α-Thioglucosides for the Preparation of Heparin Disaccharides

A. Borbás, M. Herczeg, F. Demeter, 2018, European Journal of Organic Chemistry.

Synthesis of a Heparinoid Pentasaccharide Containing l-Guluronic Acid Instead of l-Iduronic Acid with Preserved Anticoagulant Activity.

A. Borbás, K. Kövér, B. Tóth, 2022, The Journal of organic chemistry.

Synthesis of the Three Most Expensive l -Hexose Thioglycosides from d -Glucose

A. Borbás, M. Herczeg, F. Demeter, 2022, Synthesis.

Replacement of the L-iduronic acid unit of the anticoagulant pentasaccharide idraparinux by a 6-deoxy-L-talopyranose – Synthesis and conformational analysis

A. Borbás, K. Kövér, Tamás Gyöngyösi, 2018, Scientific Reports.

Simultaneous Application of Arylmethylene Acetal and Butane Diacetal Groups for Protection of Hexopyranosides: Synthesis and Chemoselective Ring-Opening Reactions.

M. Pap, A. Borbás, M. Herczeg, 2016 .

Simultaneous Application of Arylmethylene Acetal and Butane Diacetal Groups for Protection of Hexopyranosides: Synthesis and Chemoselective Ring-Opening Reactions

M. Pap, A. Borbás, M. Herczeg, 2015 .

Preparation of α-l-Rhamnobiosides by Open and Conventional Glycosylations for Studies of the rHPL Lectin

M. D. Chang, A. Borbás, Yuan-chuan Lee, 2019, Synlett.

An Efficient Synthesis of the Pentasaccharide Repeating Unit of Pseudomonas aeruginosa Psl Exopolysaccharide

M. D. Chang, A. Borbás, Yuan-chuan Lee, 2019, Synlett.

First Synthesis of DBU-Conjugated Cationic Carbohydrate Derivatives and Investigation of Their Antibacterial and Antifungal Activity

A. Borbás, J. Váradi, F. Fenyvesi, 2023, International journal of molecular sciences.

Rhamnose Binding Protein as an Anti-Bacterial Agent—Targeting Biofilm of Pseudomonas aeruginosa

C. Chiu, C. Lan, A. Borbás, 2019, Marine drugs.

Replacement of the L-iduronic acid unit of the anticoagulant pentasaccharide idraparinux by a 6-deoxy-L-talopyranose – Synthesis and conformational analysis

A. Borbás, K. Kövér, Tamás Gyöngyösi, 2018, Scientific Reports.

Synthesis of the Three Most Expensive l -Hexose Thioglycosides from d -Glucose

A. Borbás, M. Herczeg, F. Demeter, 2022, Synthesis.