The chemical synthesis of the anticodon loop of an eukaryotic initiator tRNA containing the hypermodified nucleoside N6-/N-threonylcarbonyl/-adenosine/t6A/1.

Antzeko izenburuak

• 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.
  nork: Adamiak, R W, et al.
  Argitaratua: (1977)
• Chemical modification of N(6)-/N-threonylcarbonyl/adenosine. Part I. Reaction on nucleoside level with some alkylating agents
  nork: Adamiak, R.W., et al.
  Argitaratua: (1978)
• 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.
  nork: Adamiak, R W, et al.
  Argitaratua: (1976)
• tRNA anticodon shifts in eukaryotic genomes
  nork: Rogers, Hubert H., et al.
  Argitaratua: (2014)
• Chemical modification of N6-(N-threonylcarbonyl) adenosine. Part II. Condensation of the carboxyl group with amines.
  nork: Krzyzosiak, W J, et al.
  Argitaratua: (1979)