L-threoninol as a chiral linker of azobenzene for the effective photo-regulation of DNA triplex formation

Tohru Takarada, Daisuke Tamaru, Xingguo Liang, Hiroyuki Asanuma, Makoto Komiyama

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

An azobenzene was enantioselectively attached to the 5′-end of oligo(T) through D-or L-threoninol. Photo-isomerization of azobenzene, tethered on L-threoninol, induced much larger change of melting temperature of triplex formation than did that on the D-form.

Original languageEnglish
Pages (from-to)732-733
Number of pages2
JournalChemistry Letters
Issue number7
Publication statusPublished - 2001
Externally publishedYes

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Photoisomerization
Melting point
triplex DNA
azobenzene
threoninol

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Takarada, T., Tamaru, D., Liang, X., Asanuma, H., & Komiyama, M. (2001). L-threoninol as a chiral linker of azobenzene for the effective photo-regulation of DNA triplex formation. Chemistry Letters, (7), 732-733.

L-threoninol as a chiral linker of azobenzene for the effective photo-regulation of DNA triplex formation. / Takarada, Tohru; Tamaru, Daisuke; Liang, Xingguo; Asanuma, Hiroyuki; Komiyama, Makoto.

In: Chemistry Letters, No. 7, 2001, p. 732-733.

Research output: Contribution to journalArticle

Takarada, T, Tamaru, D, Liang, X, Asanuma, H & Komiyama, M 2001, 'L-threoninol as a chiral linker of azobenzene for the effective photo-regulation of DNA triplex formation', Chemistry Letters, no. 7, pp. 732-733.
Takarada, Tohru ; Tamaru, Daisuke ; Liang, Xingguo ; Asanuma, Hiroyuki ; Komiyama, Makoto. / L-threoninol as a chiral linker of azobenzene for the effective photo-regulation of DNA triplex formation. In: Chemistry Letters. 2001 ; No. 7. pp. 732-733.
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