Action of acid on oligoribonucleotide phosphotriester intermediates. Effect of released vicinal hydroxy functions.

Eitemau Tebyg

• Nucleoside-3'-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. III. An improved preparation of nucleoside 3'-phosphotriesters, their 1H NMR characterization and new conditions for removal of 2-cyanoethyl group.
  gan: Adamiak, R W, et al.
  Cyhoeddwyd: (1976)
• New effective method for the synthesis of oligonucleotides via phosphotriester intermediates.
  gan: Efimov, V A, et al.
  Cyhoeddwyd: (1982)
• Synthesis of ppTppp via phosphotriester intermediates.
  gan: Schattenkerk, C, et al.
  Cyhoeddwyd: (1983)
• Synthesis of 3'-phosphates of diribonucleoside monophosphates via phosphotriester intermediates.
  gan: van Boom, J H, et al.
  Cyhoeddwyd: (1976)
• Solid phase synthesis of oligoribonucleotides using the 1-[(2-chloro-4-methyl)phenyl]-4-methoxypiperidin-4-yl (Ctmp) group for the protection of the 2'-hydroxy functions and the H-phosphonate approach.
  gan: Sakatsume, O, et al.
  Cyhoeddwyd: (1989)