NMR-Untersuchungen an Dicyclopentadien-Derivaten. VII. Zur Abhängigkeit des γ-gauche Effektes von der sterischen Kompression eng benachbarter Protonen bei exo/endo-Isomerieumkehr
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Wiley
Reference17 articles.
1. NMR-Untersuchungen an Dicyclopentadienderivaten: II.—13C-NMR: γ-gauche-Effekt in Abhängigkeit von derexo/endo-Isomerie an Dicyclopentadien diolen
2. Carbon-13 magnetic resonance. VII. Steric perturbation of the carbon-13 chemical shift
3. Carbon-13 chemical shifts of substituted nortricyclenes
4. Nuclear magnetic resonance spectroscopy. Carbon-13 spectra of steroids
5. Bicycloaromaticity. Stability and rearrangement of the bicyclo[3.2.2]nonatrienyl cation
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1. Synthesis and NMR spectra of the syn and anti isomers of substituted cyclobutanes—evidence for steric and spatial hyperconjugative interactions;Tetrahedron;2011-04
2. The anisotropic effect of functional groups in 1H NMR spectra is the molecular response property of spatial nucleus independent chemical shifts (NICS)—Conformational equilibria of exo/endotetrahydrodicyclopentadiene derivatives;Org. Biomol. Chem.;2011
3. Substituent Effects on13C Chemical Shifts in Aliphatic Molecular Systems. Dependence on Constitution and Stereochemistry;Topics in Stereochemistry;2007-02-26
4. Steric substituent effects on 13C nmr chemical shifts of 8-(exo/endo)-substituted 1,5-dimethylbicyclo[3.2.1]octanes;Tetrahedron;1987-01
5. Bicyclo[2.2.1]heptanes;Stereochemical Analysis of Alicyclic Compounds by C-13 NMR Spectroscopy;1987
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