ISSN:
0749-1581
Keywords:
NMR
;
substituent-induced chemical shifts
;
2-N-acetamido-2-deoxy-β-D-glucopyranosides
;
Chemistry
;
Analytical Chemistry and Spectroscopy
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
The additive behaviour generally observed for the substituent-induced chemical shifts (SCS) for disubstituted benzenes was examined for a series of aryl 2-N-acetamido-2-deoxy-β-D-glucopyranosides having a wide range of para substituents with varying possible electronic contributions. The SCS values associated with non-acetylated and peracetylated glucoside rings in para-substituted aryl 2-N-acetamido-2-deoxy-β-D-glucopyranosides were calculated. The additive nature of SCS analysis for para-substituted systems was shown to hold for the meta and para positions but the very small change in chemical shifts for the ortho positions precluded attempts at analysis of these data. The observation of a good correlation for the ipso carbons for the acetylated compounds compared with a poor correlation for the same site in the non-acetylated compounds is not well understood.
Additional Material:
3 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/mrc.1260331208
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