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

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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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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.