Oligonucleotides carrying a peptide nucleic acid (PNA) tail at the 3'-end h
ave been efficiently prepared by an on-line automated synthetic protocol ex
ploiting commercially available Bhoc/Fmoc PNA monomers for the assembly of
the PNA tract, followed by a deprotection/reprotection of the base protecti
ng groups. The syntheses of the ODN domain in the chimeras have then been p
erformed by standard methods. The hybridization properties of the synthesiz
ed chimeras with complementary DNA fragments have been investigated by ther
mal denaturation experiments. (C) 2001 Elsevier Science Ltd. All rights res
erved.