Intramolecular non-bonded interactions and β- and γ-substituent 13C NMR chemical shifts: application to series of adamantane and norbornane derivatives-Reference-Cited by-同舟云学术

Intramolecular non-bonded interactions and β- and γ-substituent 13C NMR chemical shifts: application to series of adamantane and norbornane derivatives

Published:1988-02 Issue:1-2 Volume:164 Page:189-194
ISSN:0166-1280
Container-title:Journal of Molecular Structure: THEOCHEM
language:en
Short-container-title:Journal of Molecular Structure: THEOCHEM

Author:

Pachter R.,Wessels P.L.

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference12 articles.

1. Substituent Effects on Nuclear Shielding

2. 13C chemical shifts in series of adamantane and norbornane derivatives. INDO calculations

3. Intramolecular van der waals interactions and chemical shifts: A model for β- and γ-effects

4. Intramolecular van der Waals interactions and13C chemical shifts: Substituent effects in some cyclic and bicyclic systems

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1. The ?- and the ?-effects in13C NMR spectroscopy in terms of nuclear chemical shielding (NCS) analysis JOURNAL OF PHYSICAL ORGANIC CHEMISTRYJ. Phys. Org. Chem. 2004;17: 680-685. DOI: 10.1002/poc.746;Journal of Physical Organic Chemistry;2005

2. Steric contributions to carbon-13 chemical shifts of 1- and 2-methyl adamantanes by DFT/GIAO;Journal of Molecular Structure: THEOCHEM;2001-04

3. Ab initio study of cyclic siloxanes (H2SiO)n:n = 3, 4, 5;Journal of Computational Chemistry;1996-07-15

4. Steric effects induced by solvent association.29Si NMR chemical shifts in trimethylsiloxysteroids controlled by solvent accessible surface;Magnetic Resonance in Chemistry;1994-07

5. Steric effects on NMR chemical shifts controlled by the solvent's accessible surface;J. Chem. Soc., Perkin Trans. 2;1994