N.M.R. Spectral Studies of Some Quinolone Derivatives. VIII.13C-1H Coupling Constants for the 2-Quinolone System
Author:
Publisher
Informa UK Limited
Subject
Spectroscopy,Atomic and Molecular Physics, and Optics,Analytical Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00387019408002504
Reference30 articles.
1. N.M.R. Spectral Studies of Some Quinolone Derivatives. Part VII.1Carbon-13 Magnetic Resonance Spectral Studies of N-Methyl-2-Quinolone Derivatives and an Examination ofperiSubstituent Effects
2. 13C NMR of polycyclic aromatic compounds. A review
3. Marshall, J. L. 1983.“Carbon-Carbon and Carbon-Proton NMR Couplings: Applications to Organic Stereochemistry and Conformational Analysis”, 42–64. Deerfield Beach: Verlag Chemie International.
4. 13C N.M.R spectra of quinoline and methylquinolines. The magnitude of the vicinal (peri) 3JCCCH coupling constants
5. Carbon-13 NMR spectroscopy of heterocyclic compounds—III
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1. 2-polyfluoroalkylchromones 12. Nitration of 5,7-dimethyl-2-polyhaloalkylchromones and complete assignment of signals in the H-1 and C-13 NMR spectra of 5,7-dimethyl-2-trifluromethylchromone and its mono- and dinitro derivatives;Russian Chemical Bulletin;2002
2. Re-examination of the 13C NMR spectrum of xanthene: a revised correlation for the carbocyclic ring 3JCH meta-coupling constants in fused oxygen heterocycles;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;1995-12
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