Synthesis of 5'-terminal capped oligonucleotides using O-N phosphoryl migration of phosphoramidite derivatives

Org Lett. 2012 Jan 6;14(1):10-3. doi: 10.1021/ol2026075. Epub 2011 Dec 14.

Abstract

Trivalent phosphoramidite derivatives could be readily converted by reacting with 1-hydroxy-7-azabenzotriazole to phosphotriester intermediates; these intermediates reacted smoothly with phosphorylated compounds to give pyrophosphate derivatives. This new phosphorylation approach enabled a facile and rapid synthesis of 5'-adenylated DNA oligomers (A(5')ppDNA) on resins using a silyl-type linker. Our new approach could be applied to the synthesis of a 2'-OMe-RNA oligomer containing the 5'-terminal 2,2,7-trimethylguanosine cap structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Molecular Structure
  • Oligonucleotides / chemical synthesis*
  • Organophosphorus Compounds / chemistry*
  • Phosphorylation

Substances

  • Oligonucleotides
  • Organophosphorus Compounds
  • phosphoramidite