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.

Ítems similars

• Chromatography on Sephadex LH20 as an efficient purification step after removal of internucleotide 2,2,2-trichloroethyl protective groups from oligoribonucleotide phosphotriesters.
  per: Grześkowiak, K, et al.
  Publicat: (1980)
• 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.
  per: Adamiak, R W, et al.
  Publicat: (1976)
• The chemical synthesis of the anticodon loop of an eukaryotic initiator tRNA containing the hypermodified nucleoside N6-/N-threonylcarbonyl/-adenosine/t6A/1.
  per: Adamiak, R W, et al.
  Publicat: (1978)
• Association of 2'-5' oligoribonucleotides.
  per: Kierzek, R, et al.
  Publicat: (1992)
• A new type of silyl protecting groups in nucleoside chemistry
  per: Markiewicz, W.T., et al.
  Publicat: (1978)