György Hodosi

A Fundamentally New, Simple, Stereospecific Synthesis of Oligosaccharides Containing the β-Mannopyranosyl and β-Rhamnopyranosyl Linkage

György Hodosi, P Kováč · Journal of the American Chemical Society · 1997 · 122 citations

Biosynthesis, Bioorganic Chemistry, Stereospecific Synthesis +15

Glycosylation via locked anomeric configuration: stereospecific synthesis of oligosaccharides containing the β-d-mannopyranosyl and β-l-rhamnopyranosyl linkage11For a preliminary account of this work, see ref. [7].

György Hodosi, P Kováč · Carbohydrate Research · 1998 · 57 citations

Protein Glycosylation, Bioorganic Chemistry, Stereospecific Synthesis +11

The mechanism of the hydroxyl → halogen exchange reaction in the presence of triphenylphosphine, N-bromosuccinimide, and N,N-dimethylformamide: application of a new Vilsmeier-type reagent in carbohydrate chemistry

György Hodosi, Benjamin Podányi, János Kuszmann · Carbohydrate Research · 1992 · 35 citations

Engineering, New Vilsmeier-type Reagent, Organic Chemistry +6

Polymer-supported solution synthesis of oligosaccharides: Probing glycosylations of MPEG-DOX-OH with 2-acetamidoglycopyranosyl derivatives

György Hodosi, Jiří J. Křepinský · Synlett · 1996 · 19 citations

Bioorganic Chemistry, Engineering, Glycobiology +17

Manipulation of free carbohydrates via stannylene acetals. Preparation of β-per-O-acyl derivatives of d-mannose, l-rhamnose, 6-O-trityl-d-talose, and d-lyxose

György Hodosi, Pavol Kováč · Carbohydrate Research · 1997 · 18 citations

Bioorganic Chemistry, β-Per-o-acyl Derivatives, Engineering +9