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

Authors :: López MA
Rodríguez Z
González M
Tolón B
Avila R
Mamposo T
Vélez H
Fini A
Source :: Magnetic resonance in chemistry : MRC [Magn Reson Chem] 2005 Mar; Vol. 43 (3), pp. 261-3.
Publication Year :: 2005
Abstract: 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.<br /> (Copyright 2004 John Wiley & Sons, Ltd.)

Subjects :: Cephalosporins analysis
Cephalosporins classification
Italy
Carbon Isotopes
Cephalosporins chemistry
Cephalosporins standards
Magnetic Resonance Spectroscopy methods
Magnetic Resonance Spectroscopy standards
Protons
Reference Values

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