Molecular design of novel spin-labeled nucleosides directly attached base moiety.

Toshiyuki Kaneko, Toshinori Katsurabara, Yasuhiro Matsui, Mariko Aso, Noboru Koga, Hiroshi Suemune

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

N-tert-Butylaminoxyl nucleosides (1 and 2) were synthesized starting from 6-chloropurine derivative (3). These compounds are expected as a new tool to elucidate structure of DNA. Their properties and pH-dependent change of EPR spectra were studied.

Original languageEnglish
Pages (from-to)5-6
Number of pages2
JournalNucleic acids symposium series (2004)
Issue number48
Publication statusPublished - Jan 1 2004

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Nucleosides
DNA
6-chloropurine

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

Kaneko, T., Katsurabara, T., Matsui, Y., Aso, M., Koga, N., & Suemune, H. (2004). Molecular design of novel spin-labeled nucleosides directly attached base moiety. Nucleic acids symposium series (2004), (48), 5-6.

Molecular design of novel spin-labeled nucleosides directly attached base moiety. / Kaneko, Toshiyuki; Katsurabara, Toshinori; Matsui, Yasuhiro; Aso, Mariko; Koga, Noboru; Suemune, Hiroshi.

In: Nucleic acids symposium series (2004), No. 48, 01.01.2004, p. 5-6.

Research output: Contribution to journalArticle

Kaneko, T, Katsurabara, T, Matsui, Y, Aso, M, Koga, N & Suemune, H 2004, 'Molecular design of novel spin-labeled nucleosides directly attached base moiety.', Nucleic acids symposium series (2004), no. 48, pp. 5-6.
Kaneko, Toshiyuki ; Katsurabara, Toshinori ; Matsui, Yasuhiro ; Aso, Mariko ; Koga, Noboru ; Suemune, Hiroshi. / Molecular design of novel spin-labeled nucleosides directly attached base moiety. In: Nucleic acids symposium series (2004). 2004 ; No. 48. pp. 5-6.
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