Peptide Nucleic Acid Synthesis by Novel Amide Formation
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Synthesis of self-activated peptide nucleic acid (PNA) monomers and an efficient method for PNA synthesis using a benzothiazole-2-sulfonyl(Bts) group as an amine-protecting group as well as an acid-activating group are reported. Couplings were complete within 120 min, and thedeprotection was performed in 10 min. This Bts strategy provides a high purity PNA oligomer and is appropriate for large-scale synthesis. Theresults of the 15-mer PNA oligomer are described.

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