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

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 journal › Article › peer-review

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 language	English
Pages (from-to)	732-733
Number of pages	2
Journal	Chemistry Letters
Issue number	7
Publication status	Published - 2001
Externally published	Yes

All Science Journal Classification (ASJC) codes

Chemistry(all)

Cite this

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

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.",

author = "Tohru Takarada and Daisuke Tamaru and Xingguo Liang and Hiroyuki Asanuma and Makoto Komiyama",

year = "2001",

language = "English",

pages = "732--733",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "The Chemical Society of Japan",

number = "7",

}

TY - JOUR

T1 - L-threoninol as a chiral linker of azobenzene for the effective photo-regulation of DNA triplex formation

AU - Takarada, Tohru

AU - Tamaru, Daisuke

AU - Liang, Xingguo

AU - Asanuma, Hiroyuki

AU - Komiyama, Makoto

PY - 2001

Y1 - 2001

N2 - 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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=0035645176&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0035645176&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0035645176

SN - 0366-7022

SP - 732

EP - 733

JO - Chemistry Letters

JF - Chemistry Letters

IS - 7

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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