For synthesis of N-7-cyanoborane-containing oligonucleotides, the 5'-D
MT protecting group is not a suitable precursor because the boronated
nucleoside is incompatible with DMT cations released during deprotecti
on of the oligonucleotide. As an alternative to DMT, we have investiga
ted use of the 5'-Fmoc protecting group. We found that the cyanoborane
group is stable during synthesis and deprotection conditions used wit
h Fmoc derivatives.