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1H and 13C spectral assignments of 7β-(cinnamoyl-substituted)amino-3-acetoxymethyl-cephalosporins

✍ Scribed by Miguel A. López; Zalua Rodríguez; Maritza González; Blanca Tolón; Rizette Avila; Taimirys Mamposo; Hermán Vélez; Adamo Fini

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
89 KB
Volume
43
Category
Article
ISSN
0749-1581

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✦ Synopsis

Abstract

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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