Novel consecutive β- and γ-turn mimetics composed of α-aminooxy tripeptides

Bong Hyeon Baek, Myung Ryul Lee, Kwang Yon Kim, Ung In Cho, Doo Wan Boo, Injae Shin

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

(Matrix presented) To develop novel consecutive β- and γ-turn mimetics, we designed and characterized α-aminooxy tripeptides (trimers) consisting of oxanipecotic acid dimer and α-aminooxy acid. According to FT-IR and NMR data, as well as ab initio quantum calculations, the trimers adopted unusual folded structures with consecutive β- and γ-turnlike conformations.

Original languageEnglish
Pages (from-to)971-974
Number of pages4
JournalOrganic Letters
Volume5
Issue number7
DOIs
Publication statusPublished - 2003 Apr 3

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trimers
acids
Acids
Dimers
Conformations
dimers
Nuclear magnetic resonance
nuclear magnetic resonance
matrices

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Baek, Bong Hyeon ; Lee, Myung Ryul ; Kim, Kwang Yon ; Cho, Ung In ; Boo, Doo Wan ; Shin, Injae. / Novel consecutive β- and γ-turn mimetics composed of α-aminooxy tripeptides. In: Organic Letters. 2003 ; Vol. 5, No. 7. pp. 971-974.
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Novel consecutive β- and γ-turn mimetics composed of α-aminooxy tripeptides. / Baek, Bong Hyeon; Lee, Myung Ryul; Kim, Kwang Yon; Cho, Ung In; Boo, Doo Wan; Shin, Injae.

In: Organic Letters, Vol. 5, No. 7, 03.04.2003, p. 971-974.

Research output: Contribution to journalArticle

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AU - Lee, Myung Ryul

AU - Kim, Kwang Yon

AU - Cho, Ung In

AU - Boo, Doo Wan

AU - Shin, Injae

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