On the use of partly resolved structure for the analysis of NMR spectra. Application to the determination of the signs of the hydroxyl proton-ring proton nuclear spin coupling constants in substituted phenols
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Spectroscopy,Atomic and Molecular Physics, and Optics
Reference25 articles.
1. Analysis of Weakly Coupled Nuclear Magnetic Resonance Spectra: Methyl Salicylate
2. Hydrogen Bonding and Stereospecific Long-range Spin Coupling in 3-Nitro- and 5-Nitrosalicylaldehyde.
3. Proton Chemical Shifts, Long-Range Spin Coupling, and pi-Electron Distributions in Methoxy Derivatives of Salicylaldehyde and o-Hydroxyacetophenone.
4. Proton spin coupling through five chemical bonds
5. (H, H) coupling constants in the nuclear magnetic resonance spectra of hydrocarbon groupings
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2. 17O, 1H coupling constants in intramolecular hydrogen bonds;Chemical Physics Letters;1990-11
3. Concerning in 2-methylphenol and its derivatives. A proximate coupling;Canadian Journal of Chemistry;1985-03-01
4. Conformational preference of substituted naphthalenes. 2—proton-proton coupling constants of hydroxy derivatives of naphthalene;Organic Magnetic Resonance;1984-06
5. Spin–spin coupling between hydroxyl and aldehydic protons in some salicylaldehyde derivatives. Correlation with the hydroxyl proton chemical shift;Canadian Journal of Chemistry;1984-02-01
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