189159-91-9Relevant articles and documents
Introduction of a universal solid support for oligonucleotide synthesis
Scheuer-Larsen, Claus,Rosenbohm, Christoph,Jorgensen, Thomas J. D.,Wengel, Jesper
, p. 67 - 80 (2007/10/03)
Protection of 1,4-anhydro-D-ribitol with the bidentate reagent 1,3- dichloro-1,1,3,3-tetraisopropyldisiloxane, followed by 4,4'- dimethoxytritylation, selective cleavage of the silyl group at the secondary oxygen, chloroacetylation, and desilylation at the 5-position, afforded 1,4- anhydro-3-O-chloroacetyl-2-O-(4,4'-dimethoxytrityl)-D-ribitol. Derivatisation of the free hydroxyl group with LCAA-CPG gave a novel universal solid support for use in oligonucleotide synthesis and phosphoramidite-based combinatorial chemistry. This solid support was used for synthesis of a number of oligonucleotides, for which the purity and identity with oligonucleotides synthesised on commercial supports was demonstrated.