Synthesis of an artificial oligonucleotide an efficient cycloaddition reaction.

Tomoko Fujino, Guillot Marine, Eiichi Nakamura

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

We developed a new class of artificial oligonucleotides bearing triazole linkers between furanose-like cyclic structures with nucleobase. Elongation reaction of the oligonucleotide was achieved efficiently by [3 + 2] cycloaddition reaction between acetylene and azide.

Original languageEnglish
Pages (from-to)267-268
Number of pages2
JournalNucleic acids symposium series (2004)
Issue number51
DOIs
Publication statusPublished - 2007

ASJC Scopus subject areas

  • Medicine(all)

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