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.

1H and 13 C spectral assignments of 7beta-(cinnamoyl-substituted)amino-3-acetoxymethyl-cephalosporins / Lopez M.A.; Rodriguez Z.; Gonzalez M.; Tolon B.; Avila R.; Mamposo T.; Velez H.; Fini A.. - In: MAGNETIC RESONANCE IN CHEMISTRY. - ISSN 0749-1581. - STAMPA. - 43:(2005), pp. 261-263. [10.1002/mrc.1525]

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

FINI, ADAMO
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. Copyright 2004 John Wiley & Sons, Ltd.
2005
1H and 13 C spectral assignments of 7beta-(cinnamoyl-substituted)amino-3-acetoxymethyl-cephalosporins / Lopez M.A.; Rodriguez Z.; Gonzalez M.; Tolon B.; Avila R.; Mamposo T.; Velez H.; Fini A.. - In: MAGNETIC RESONANCE IN CHEMISTRY. - ISSN 0749-1581. - STAMPA. - 43:(2005), pp. 261-263. [10.1002/mrc.1525]
Lopez M.A.; Rodriguez Z.; Gonzalez M.; Tolon B.; Avila R.; Mamposo T.; Velez H.; Fini A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/11890
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