Method for the Diastereoselective Synthesis of Pronucleotides
The present invention is directed to a process for the diastereoselective synthesis of phosphorus compounds, particularly pronucleotides (nucleotide prorugs).
Pronucleotides represent a promising alternative to improve the biological activity of nucleoside analogs in antiviral and cancer chemotherapy.
Weitere Informationen: PDF
TuTech Innovation GmbH (TuTech)
Tel.: +49 40 76629-6541
Ansprechpartner
Dr. Markus Kähler, Astrid Stichnoth, Karl-Heinz Rehfeldt, Dr. Torsten Stachelhaus, Dr. Nico Steiert
