13C nuclear magnetic resonance spectra. XV—the γ-anti substituent effect and its dependence on substitution at the α- and γ-carbon atom-Reference-Cited by-同舟云学术

13C nuclear magnetic resonance spectra. XV—the γ-anti substituent effect and its dependence on substitution at the α- and γ-carbon atom

Published:1981-05 Issue:1 Volume:16 Page:32-35
ISSN:0030-4921
Container-title:Organic Magnetic Resonance
language:en
Short-container-title:Org. Magn. Reson.

Author:

Duddeck Helmut,Islam Md. Rabiul

Publisher

Wiley

Subject

General Materials Science,General Chemistry,General Materials Science,General Chemistry

Reference31 articles.

1. For Part XIV, see and Tetrahedron, in press.

2. See for example and Stereochemical aspects of 13C NMR spectroscopy. In Topics in Stereochemistry, ed. by and Vol. 8, p. 1. Wiley-Interscience, New York (1973).

3. Carbon-13 magnetic resonance. Upfield shifts caused by nitrogen, oxygen, and fluorine atoms located at the .gamma. position and antiperiplanar to the nucleus observed

4. Concerning stereochemical assignments from 13C spectra of systems experiencing γ substituent effects. Deshielding antiperiplanar interactions can mislead the unwary

5. Carbon-13 NMR studies. 73—carbon-13 spectra of several 10-methyl-trans-decalins. Further definition of the deshielding antiperiplanar γ effect

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