[GRAPHICS]
A new scheme for the synthesis of peptide nucleic acid (PNA) is described.
First, a resin-bound amino acid is alkylated under Fukuyama-Mitsunobu condi
tions. A nucleobase is then incorporated via an acid fluoride. Subsequently
, oligomerization may be achieved by deprotection, coupling of another amin
o acid, and repetition of the cycle. Each step of the submonomer synthesis
has been optimized to provide essentially quantitative yield.