1H NMR utilization of through-space effects: III—configuration of oximes and analogous compounds
Author:
Publisher
Wiley
Subject
General Materials Science,General Chemistry,General Materials Science,General Chemistry
Reference14 articles.
1. 1H NMR utilization of through-space effects in configurational assignments. I—application to nitriles; determination of the separate effects of the electric field and anisotropy of the CN group
2. 1H NMR utilization of through-space effects. II—conformation of dienic ketones
3. Oxime hydrochlorides. IV. Nuclear magnetic resonance studies of the stereochemistry of 2-substituted cyclohexanone oximes and their hydrochlorides. Conformation change caused by protonation and hydrogen bonding
4. Theory of Nuclear Magnetic Shielding in Molecules. I. Long‐Range Dipolar Shielding of Protons
5. CHEMICAL SHIFTS IN THE NUCLEAR MAGNETIC RESONANCE SPECTRA OF MOLECULES CONTAINING POLAR GROUPS
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5. Axial/equatorial populations in ?-hetero-substituted cyclohexanone Oximes andO-methyl oximes;Magnetic Resonance in Chemistry;2000
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