1H and 13 C spectral assignments of 7beta-(cinnamoyl-substituted)amino-3-acetoxymethyl-cephalosporins.
| Autor: | López MA; Centro de Química Farmacéutica, Avenida 200 y 21, Siboney, Playa, CP 16042, Ciudad de La Habana, Cuba., Rodríguez Z, González M, Tolón B, Avila R, Mamposo T, Vélez H, Fini A |
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| Jazyk: | angličtina |
| Zdroj: | Magnetic resonance in chemistry : MRC [Magn Reson Chem] 2005 Mar; Vol. 43 (3), pp. 261-3. |
| DOI: | 10.1002/mrc.1525 |
| Abstrakt: | The (1)H and (13)C spectroscopic data for 7beta-(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 alpha-position of the cinnamoyl moiety has little influence on the spectroscopic properties of the 7beta-aminocephalosporanic acid parent moiety. (Copyright 2004 John Wiley & Sons, Ltd.) |
| Databáze: | MEDLINE |
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