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Relative configuration of micrograms of natural compounds using proton residual chemical shift anisotropy
Nath, N.; Fuentes-Monteverde, J.C.; Pech-Puch, D.; Rodríguez, J.; Jimenez, C.; Noll, M.; Kreiter, A.; Reggelin, M.; Navarro-Vázquez, A.; Griesinger, C. (2020). Relative configuration of micrograms of natural compounds using proton residual chemical shift anisotropy. Nature Comm. 11(1): 9 pp. https://dx.doi.org/10.1038/s41467-020-18093-5
In: Nature Communications. Nature Publishing Group: London. ISSN 2041-1723; e-ISSN 2041-1723, meer
Peer reviewed article  
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  • Nath, N.
  • Fuentes-Monteverde, J.C.
  • Pech-Puch, D.
  • Rodríguez, J.
  • Jimenez, C., meer
  • Noll, M.
  • Kreiter, A.
  • Reggelin, M.
  • Navarro-Vázquez, A.
  • Griesinger, C.
Abstract
    3D molecular structure determination is a challenge for organic compounds or natural products available in minute amounts. Proton/proton and proton/carbon correlations yield the constitution. J couplings and NOEs oftentimes supported by one-bond 1H,13C residual dipolar couplings (RDCs) or by 13C residual chemical shift anisotropies (RCSAs) provide the relative configuration. However, these RDCs or carbon RCSAs rely on 1% natural abundance of 13C preventing their use for compounds available only in quantities of a few 10’s of µgs. By contrast, 1H RCSAs provide similar information on spatial orientation of structural moieties within a molecule, while using the abundant 1H spin. Herein, 1H RCSAs are accurately measured using constrained aligning gels or liquid crystals and applied to the 3D structural determination of molecules with varying complexities. Even more, deuterated alignment media allow the elucidation of the relative configuration of around 35 µg of a briarane compound isolated from Briareum asbestinum.
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