Synthesis of an artificial oligonucleotide an efficient cycloaddition reaction.

Tomoko Fujino; Guillot Marine; Eiichi Nakamura

doi:10.1093/nass/nrm134

Synthesis of an artificial oligonucleotide an efficient cycloaddition reaction.

Tomoko Fujino, Guillot Marine, Eiichi Nakamura

SCI - Chemistry

Research output: Contribution to journal › Article › peer-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 language	English
Pages (from-to)	267-268
Number of pages	2
Journal	Nucleic acids symposium series (2004)
Issue number	51
DOIs	https://doi.org/10.1093/nass/nrm134
Publication status	Published - 2007

ASJC Scopus subject areas

Medicine(all)

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10.1093/nass/nrm134

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title = "Synthesis of an artificial oligonucleotide an efficient cycloaddition reaction.",

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.",

author = "Tomoko Fujino and Guillot Marine and Eiichi Nakamura",

year = "2007",

doi = "10.1093/nass/nrm134",

language = "English",

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journal = "Nucleic acids symposium series (2004)",

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AU - Marine, Guillot

AU - Nakamura, Eiichi

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JF - Nucleic acids symposium series (2004)

SN - 1746-8272

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ER -

Synthesis of an artificial oligonucleotide an efficient cycloaddition reaction.

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