Reusable solid-phase supports for large scale oligonucleotide synthesis hav
e been prepared by converting amino derivatized supports into hydroxyl supp
orts. Rapid nucleoside attachment, via a Q-linker arm, was automatically pe
rformed on the DNA synthesizer using HBTU and DMAP as the coupling reagents
. All steps were suitable for automation and similar to 1.5 h was required
to prepare the supports for reuse. Up to twelve consecutive syntheses of a
20-mer phosphorothioate were performed on a synthesis column.