Efficient cross-linking reactions by functional nucleobases capable of in situ activation under neutral conditions.

Fumi Nagatsugi, Yasushi Suenaga, Shigeki Sasaki

Research output: Contribution to journalArticle

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Abstract

We have previously described that the oligonucleotides containing phenylsulfide derivatives of 2-amino-6-vinylpurine nucleoside analog are activated within duplex to form cross-link toward cytidine selectively at the target site. However, the cross-linking reaction via the in-situ activation needs acidic conditions. In this paper, we wish to report that the new 2-amino-6-vinylpurine derivatives designed to have a structure of "double-activation" for in-situ activation exhibit fast cross-linking with cytidine under neutral conditions.

Original languageEnglish
Pages (from-to)155-156
Number of pages2
JournalNucleic acids research. Supplement (2001)
Issue number3
Publication statusPublished - Jan 1 2003

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Cytidine
Cross Reactions
Nucleosides
Oligonucleotides
2-amino-6-vinylpurine

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Efficient cross-linking reactions by functional nucleobases capable of in situ activation under neutral conditions. / Nagatsugi, Fumi; Suenaga, Yasushi; Sasaki, Shigeki.

In: Nucleic acids research. Supplement (2001), No. 3, 01.01.2003, p. 155-156.

Research output: Contribution to journalArticle

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