Studies on the t-butyldimethylsilyl group as 2'-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach.

Ítems similars

• Evaluation of 2'-hydroxyl protection in RNA-synthesis using the H-phosphonate approach.
  per: Rozners, E, et al.
  Publicat: (1994)
• Solid phase synthesis of oligoribonucleotides using the o-nitrobenzyl group for 2'-hydroxyl protection and H-phosphonate chemistry.
  per: Tanaka, T, et al.
  Publicat: (1987)
• The H-phosphonate approach to the solution phase synthesis of linear and cyclic oligoribonucleotides.
  per: Reese, C B, et al.
  Publicat: (1999)
• Removal of t-butyldimethylsilyl protection in RNA-synthesis. Triethylamine trihydrofluoride (TEA, 3HF) is a more reliable alternative to tetrabutylammonium fluoride (TBAF).
  per: Westman, E, et al.
  Publicat: (1994)
• 5'-Levulinyl and 2'-tetrahydrofuranyl protection for the synthesis of oligoribonucleotides by the phosphoramidite approach.
  per: Iwai, S, et al.
  Publicat: (1988)