Synthese monofluorierter cyclopropanoider Nucleosidanaloga Synthesis of Monofluorinated Cyclopropanoid Nucleoside Analogues Rene´ Csuk und Gisela Thiede

The work in this dissertation revealed alteration in the expression of two junctional proteins, connexin43 and N-cadherin, and one intermediate filament protein,

A number of new substituted 1,2,4-triazole {[(1,2,4-triazolyl)ethyl]tetrazolyl} derivatives, their sugar hydrazones, and their acyclic C-nucleoside analogues were

The reaction of methyl 4,6-O-benzylidene-2-deoxy- α - D -erythro-hexopyranosid-3-ulose (1) with ethynylmagnesium bromide in tetrahydrofuran and subsequent trimethylsilylation

All nucleosides are evaluated by an enzymatic assay to be substrates of herpes simplex virus type 1 thymidine kinase (HSV-1 TK) and compared with uridine, thymidine

Transferhydrogenolytische Debenzylierung (AAV3) Zu einer Lösung des Benzylethers in Methanol wurden Pearlmans Katalysator und Cyclohexen gegeben und dieses Reaktionsgemisch

A novel class of nucleoside analogues containing adenine, uracil, thymine and 5-fluoro- uracil as the heterocyclic moieties have been prepared from 2-phenylcyclopropane carboxylic

Experimental data of selected examples reflecting the characteristic behavior of transglycosylation systems depending on the thermodynamic properties of the

Finally, the Federal Fiscal Court points to the fact that split- ting the authority to dispose of a physical object with the effect that several persons are entitled