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dc.Type: research-article
dc.Title: Determination of Relative Configuration from Residual Chemical Shift Anisotropy
dc.Identifier: 10.1021/jacs.6b04082
title: Determination of Relative Configuration from Residual Chemical Shift Anisotropy - Journal of the American Chemical Society (ACS Publications)
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dc.Publisher: American Chemical Society
dc.Language: EN
dc.Description: Determination of relative configuration is frequently a rate-limiting step in the characterization of small organic molecules. Solution NMR-based nuclear Overhauser effect and scalar J-coupling constants can provide useful spatial information but often fail when stereocenters are separated by more than 4?5 Å. Residual dipolar couplings (RDCs) can provide a means of assigning relative configuration without limits of distance between stereocenters. However, sensitivity limits their application. Chemical shift is the most readily measured NMR parameter, and partial molecular alignment can reveal the anisotropic component of the chemical shift tensor, manifested as residual chemical shift anisotropy (RCSA). Hence, 13C RCSAs provide information on the relative orientations of specific structural moieties including nonprotonated carbons and can be used for stereochemical assignment. Herein, we present two robust and sensitive methods to accurately measure and apply 13C RCSAs for stereochemical assignment. The c...
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dc:title: Determination of Relative Configuration from Residual Chemical Shift Anisotropy - Journal of the American Chemical Society (ACS Publications)
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dc.Creator: Nilamoni Nath
dc.Date: July 22, 2016
dc.Coverage: world
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