Synthetic studies on nucleoside 5'-H-phosphonate monoesters under Mitsunobu reaction conditions

Studies on the Alkylation of 5'-CMP under Alkaline Conditions

The reaction o f 5'-CMP with methyl, ethyl, «-propyl and isopropyl iodides gave predomi­ nantly ribose alkylated products. Various alkylated derivatives have been characterized using UV spectroscopy, paper electrophoresis, 'H N M R and FAB (negative) mass spectroscopic techniques. Under strongly alkaline conditions the 2'-0-alkylated derivatives are synthesized in maximal yields. Isopropylation...

Studies on Oxidative Couplings in H-Phosphonate Chemistry

In this thesis oxidative coupling of H-phosphonate and H-phosphonothioate diesters with different alcohols and amines are presented. Since the reactions with alcohols previously have been particularly unfavourable due to competing side reactions, a modified protocol leading to high coupling yields of structurally diverse hydroxylic components was developed. The phosphorylation reaction was stud...

Tetrametallic lanthanide(III) phosphonate cages: synthetic, structural and magnetic studies.

The synthesis, structures and magnetic properties of a family of lanthanide complexes containing phosphonate ligands are reported. Reaction of hydrated lanthanide nitrate and (t)butylphosphonic acid under reflux conditions in iso-butanol, in the presence of pivalic acid as a co-ligand produced five new lanthanide complexes; pyridine (py) was present as a base. The compounds formed are tetrameta...

Synthesis of Nucleoside Phosphate and Phosphonate Prodrugs

Phosphonate monoesters on a thiacalix[4]arene framework as potential inhibitors of protein tyrosine phosphatase 1B.

Monoester derivatives of thiacalix[4]arene tetrakis(methylphosphonic) acid were found to be capable of inhibiting protein tyrosine phosphatase 1B. In addition, these compounds can strongly bind to human serum albumin.