Conformational Plasticity in Glycomimetics: Fluorocarbamethyl‐L‐idopyranosides Mimic the Intrinsic Dynamic Behaviour of Natural Idose Rings. Issue 29 (10th June 2015)
- Record Type:
- Journal Article
- Title:
- Conformational Plasticity in Glycomimetics: Fluorocarbamethyl‐L‐idopyranosides Mimic the Intrinsic Dynamic Behaviour of Natural Idose Rings. Issue 29 (10th June 2015)
- Main Title:
- Conformational Plasticity in Glycomimetics: Fluorocarbamethyl‐L‐idopyranosides Mimic the Intrinsic Dynamic Behaviour of Natural Idose Rings
- Authors:
- Unione, Luca
Xu, Bixue
Díaz, Dolores
Martín‐Santamaría, Sonsoles
Poveda, Ana
Sardinha, João
Rauter, Amelia Pilar
Blériot, Yves
Zhang, Yongmin
Cañada, F. Javier
Sollogoub, Matthieu
Jiménez‐Barbero, Jesus - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Sugar function, structure and dynamics are intricately correlated. Ring flexibility is intrinsically related to biological activity; actually plasticity in <sc>L</sc>‐iduronic rings modulates their interactions with biological receptors. However, the access to the experimental values of the energy barriers and free‐energy difference for conformer interconversion in water solution has been elusive. Here, a new generation of fluorine‐containing glycomimetics is presented. We have applied a combination of organic synthesis, NMR spectroscopy and computational methods to investigate the conformational behaviour of idose‐ and glucose‐like rings. We have used low‐temperature NMR spectroscopic experiments to slow down the conformational exchange of the idose‐like rings. Under these conditions, the exchange rate becomes slow in the <sup>19</sup>F NMR spectroscopic chemical shift timescale and allows shedding light on the thermodynamic and kinetic features of the equilibrium. Despite the minimal structural differences between these compounds, a remarkable difference in their dynamic behaviour indeed occurs. The importance of introducing fluorine atoms in these sugars mimics is also highlighted. Only the use of <sup>19</sup>F NMR spectroscopic experiments has permitted the unveiling of key features of the conformational equilibrium that would have otherwise remained unobserved.</p> </abstract>
- Is Part Of:
- Chemistry. Volume 21:Issue 29(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 29(2015)
- Issue Display:
- Volume 21, Issue 29 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 29
- Issue Sort Value:
- 2015-0021-0029-0000
- Page Start:
- 10513
- Page End:
- 10521
- Publication Date:
- 2015-06-10
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201501249 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3611.xml