L-Threoninol as a Chiral Linker of Azobenzene for the Effective Photo-regulation of DNA Triplex Formation
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.
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Veröffentlicht in: | Chemistry letters 2001-07, Vol.30 (7), p.732-733 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.2001.732 |