1219089-91-4Relevant articles and documents
Streamlined process for the chemical synthesis of RNA using 2-O-thionocarbamate-protected nucleoside phosphoramidites in the solid phase
Dellinger, Douglas J.,Timar, Zoltan,Myerson, Joel,Sierzchala, Agnieszka B.,Turner, John,Ferreira, Fernando,Kupihar, Zoltan,Dellinger, Geraldine,Hill, Kenneth W.,Powell, James A.,Sampson, Jeffrey R.,Caruthers, Marvin H.
, p. 11540 - 11556 (2011/09/21)
An improved method for the chemical synthesis of RNA was developed utilizing a streamlined method for the preparation of phosphoramidite monomers and a single-step deprotection of the resulting oligoribonucleotide product using 1,2-diamines under anhydrous conditions. The process is compatible with most standard heterobase protection and employs a 2′-O-(1,1-dioxo- 1λ6-thiomorpholine-4-carbothioate) as a unique 2′-hydroxyl protective group. Using this approach, it was demonstrated that the chemical synthesis of RNA can be as simple and robust as the chemical synthesis of DNA.