## REFERENCE DATA carbons, for various substituent groups and positions were carried out by gated decoupling with NOE. ## RESULTS AND DISCUSSION The I3C NMR chemical shifts of the compounds are shown in Tables 123; 'J(CH) and long-range coupling constants of 2, 9, 13 and 18, measured by gated d
1H, 13C and 15N NMR spectra of ciprofloxacin
✍ Scribed by Andrzej Ziȩba; Andrzej Maślankiewicz; Jerzy Sitkowski
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 103 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1468
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✦ Synopsis
Abstract
^1^H NMR assignment, including the values of δ~H~ and J(H,H) for the cyclopropane moiety, and ^13^C NMR and ^15^N NMR spectral data for ciprofloxacin are presented. Copyright © 2004 John Wiley & Sons, Ltd.
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