Mild basic and highly selective hydrolysis of an aryl-alkyl 1-H-phosphonate diester: Preparation of the mono-1-H-phosphonylated dipeptide Z-ser(OPO2H2)-tyr(OH)NH2.

This publication has 15 references indexed in Scilit:

• A model study directed towards the preparation of nucleopeptidesviaH-phosphonate intermediates
  Nucleic Acids Research, 1987
• The organic chemistry underlying DNA synthesis
  Bioorganic Chemistry, 1986
• Synthesis of DNA via deoxynudeoside H-phosphonate Intermediates
  Nucleic Acids Research, 1986
• Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approach
  Tetrahedron Letters, 1986
• Acylphosphonates. 4. Synthesis of dithymidine phosphonate. A new method for generation of phosphonate function via aroylphosphonate intermediates
  The Journal of Organic Chemistry, 1984
• Bis[2,2,2-trifluoroethyl] Phosphite, a New Reagent for Synthesizing Mono- and Diesters of Phosphorous Acid
  Synthesis, 1984
• Some observations relating to the oximate ion promoted unblocking of oligonucleotide aryl esters
  Nucleic Acids Research, 1981
• The chemical synthesis of oligo- and poly-nucleotides by the phosphotriester approach
  Tetrahedron, 1978
• Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives
  Journal of the American Chemical Society, 1972
• Conversion of Tertiary Phosphites to Secondary Phosphonates. Diphenyl Phosphonate¹
  Journal of the American Chemical Society, 1959