1 H and 13 C spectral assignments of 7β‐(cinnamoyl‐substituted)amino‐3‐acetoxymethyl‐cephalosporins
The 1 H and 13 C spectroscopic data for 7β‐(cinnamoyl‐substituted)amino‐3‐acetoxymethyl‐cephalosporins were fully assigned by a combination of one‐ and two‐dimensional experiments. Substitution on the aromatic ring and on the double‐bond α‐position of the cinnamoyl moiety has little influence on the...
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| Veröffentlicht in: | Magnetic resonance in chemistry 2005-03, Vol.43 (3), p.261-263 |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | The
1
H and
13
C spectroscopic data for 7β‐(cinnamoyl‐substituted)amino‐3‐acetoxymethyl‐cephalosporins were fully assigned by a combination of one‐ and two‐dimensional experiments. Substitution on the aromatic ring and on the double‐bond α‐position of the cinnamoyl moiety has little influence on the spectroscopic properties of the 7β‐aminocephalosporanic acid parent moiety. Copyright © 2004 John Wiley & Sons, Ltd. |
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| ISSN: | 0749-1581 1097-458X |
| DOI: | 10.1002/mrc.1525 |