Electronic interactions implied by the non-additivity of carbon-13 substituent parameters in 2-substituted cyclohexanones-Reference-Cited by-同舟云学术

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Electronic interactions implied by the non-additivity of carbon-13 substituent parameters in 2-substituted cyclohexanones

Published:1994-04 Issue:4 Volume:32 Page:205-209
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Basso Ernani A.,Kaiser Carlos,Rittner Roberto,Lambert Joseph B.

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Reference14 articles.

1. (a) Carbon-13 NMR Spectroscopy, Chapt. 5 and 8. Academic Press, New York (1972);.

2. (b); and Carbon-13 Nuclear Magnetic Resonance Spectroscopy, 2nd ed., Chap. 3-5. Wiley-Interscience, New York (1980);.

3. and Carbon-13 NMR Spectroscopy, 3rd ed. VCH, Weinheim (1987);.

4. and Interpretation of Carbon-13 NMR Spectra, 2nd ed. Wiley, Chichester (1988);.

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1. Strong hyperconjugative interactions limit solvent and substituent influence on conformational equilibrium: the case of cis-2-halocyclohexylamines;Beilstein Journal of Organic Chemistry;2019-04-01

2. Substituent effects in the 13C NMR chemical shifts of α-mono-substituted acetonitriles;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2007-03

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