Force field and 13C-NMR investigations of substituted cyclopentanes. A concept for the adaption of 13C NMR shifts to varying torsional arrangements in flexible conformers
- 1 January 1982
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 38 (15) , 2327-2337
- https://doi.org/10.1016/0040-4020(82)87010-5
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- 13C NMR and force field investigations of hydrindane conformationsMagnetic Resonance in Chemistry, 1982
- Equilibrium conformations of four- and five-membered cyclic molecules in the gas phase: determination and classificationChemical Reviews, 1980
- Conformational relaxation as limitation of chemical models. Empirical force field calculations and carbon-13 NMR shielding effects for some cyclohexanes, bicyclo[2.2.1]heptanes, bicyclo[3.3.1]nonane, and 11.beta.-substituted estrenesJournal of the American Chemical Society, 1979
- Conformations of Five‐Membered RingsTopics in Stereochemistry, 1979
- Conformational analysis. 130. MM2. A hydrocarbon force field utilizing V1 and V2 torsional termsJournal of the American Chemical Society, 1977
- Molecular orbital theory of the electronic structure of organic compounds. 25. Conformations of methyl- and fluoro-substituted cyclopentanes and cyclohexanesJournal of the American Chemical Society, 1976
- Molecular orbital theory of the electronic structure of organic compounds. XXIII. Pseudorotation in saturated five-membered ring compoundsJournal of the American Chemical Society, 1975
- Gleichgewichtsmessungen an diastereomeren substituierten 1.2-Dibrom-äthanenEuropean Journal of Organic Chemistry, 1972
- Conformational analysis. LX. Improved calculations of the structures and energies of hydrocarbons by the Westheimer methodJournal of the American Chemical Society, 1968
- Molecular Geometry. I. Machine Computation of the Common RingsJournal of the American Chemical Society, 1961