5'-Levulinyl and 2'-tetrahydrofuranyl protection for the synthesis of oligoribonucleotides by the phosphoramidite approach.

Ítems similars

• A new solid-phase synthesis of oligoribonucleotides by the phosphoro-p-anisidate method using tetrahydrofuranyl protection of 2'-hydroxyl groups.
  per: Iwai, S, et al.
  Publicat: (1987)
• Chemical synthesis of biologically active oligoribonucleotides using beta-cyanoethyl protected ribonucleoside phosphoramidites.
  per: Scaringe, S A, et al.
  Publicat: (1990)
• Studies on the t-butyldimethylsilyl group as 2'-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach.
  per: Stawinski, J, et al.
  Publicat: (1988)
• Synthesis of 3'-thioribonucleosides and their incorporation into oligoribonucleotides via phosphoramidite chemistry.
  per: Sun, S, et al.
  Publicat: (1997)
• An Economic and Practical Synthesis of the 2-Tetrahydrofuranyl Ether Protective Group
  per: Falck, J. R., et al.
  Publicat: (2006)