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.

Gelijkaardige items

• Nucleoside 3'-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. IV. New method for removal of 2,2,2-trichloroethyl group and 31P NMR as a new tool for analysis of deblocking of internucleotide phosphate protecting groups.
  door: Adamiak, R W, et al.
  Gepubliceerd in: (1977)
• Chromatography on Sephadex LH20 as an efficient purification step after removal of internucleotide 2,2,2-trichloroethyl protective groups from oligoribonucleotide phosphotriesters.
  door: Grześkowiak, K, et al.
  Gepubliceerd in: (1980)
• The chemical synthesis of the anticodon loop of an eukaryotic initiator tRNA containing the hypermodified nucleoside N6-/N-threonylcarbonyl/-adenosine/t6A/1.
  door: Adamiak, R W, et al.
  Gepubliceerd in: (1978)
• Action of acid on oligoribonucleotide phosphotriester intermediates. Effect of released vicinal hydroxy functions.
  door: Reese, C B, et al.
  Gepubliceerd in: (1985)
• The modified nucleosides of tRNAs. II. Synthesis of 2'-O-methylcytidylyl (3'-5') cytidine.
  door: Markiewicz, W T, et al.
  Gepubliceerd in: (1975)