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Saccharide-Dependent Induction of Chiral Helicity in Achiral Synthetic Hydrogen-Bonding Oligomers

Inouye, Masahiko, Waki, Minoru, Abe, Hajime·2004·Journal of the American Chemical Society

Abstract

Conformational transitions of biopolymers are well-known to be affected by noncovalent interactions with small molecules. We found that synthetic polymers, poly- and oligo(meta-ethynylpyridine)s, are guided to helical structures by uncharged hydrogen-bonding interactions with saccharides enclosed in the inner sphere of the polymers. Circular dichroism (CD) studies revealed that chirality of saccharide was transferred to the helical sense of the polymers. Among the n-octyl pyranosides of naturally important hexoses, beta-glucoside induced CDs most effectively. Size-regulated 18-mer and longer oligomers also showed the induced CDs similar to those for the polymers. Furthermore, native monosaccharides were extracted into less polar organic solvent with the help of the polymers, inducing similar CD signals.

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Metadata

Authors
Inouye, M., Waki, M., & Abe, H.
Venue
Journal of the American Chemical Society
Published
2004-01-30
Volume
126
Issue
7
Pages
2022-2027
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2022470095
Cited by
259
References
0
FWCI
10.80
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Saccharide-Dependent Induction of Chiral Helicity in Achiral Synthetic Hydrogen-Bonding Oligomers. https://app.cochat.ai/papers/10.1021/ja039371g
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Inouye, M., Waki, M., & Abe, H. (2004). Saccharide-Dependent Induction of Chiral Helicity in Achiral Synthetic Hydrogen-Bonding Oligomers. Journal of the American Chemical Society. https://doi.org/10.1021/ja039371g

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