The relationship between proton-proton NMR coupling constants and substituent electronegativities. II—conformational analysis of the sugar ring in nucleosides and nucleotides in solution using a generalized Karplus equation-Reference-Cited by-同舟云学术

The relationship between proton-proton NMR coupling constants and substituent electronegativities. II—conformational analysis of the sugar ring in nucleosides and nucleotides in solution using a generalized Karplus equation

Published:1981-01 Issue:1 Volume:15 Page:43-52
ISSN:0030-4921
Container-title:Organic Magnetic Resonance
language:en
Short-container-title:Org. Magn. Reson.

Author:

Haasnoot C. A. G.,de Leeuw F. A. A. M.,de Leeuw H. P. M.,Altona C.

Publisher

Wiley

Subject

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

Reference42 articles.

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2. Empirical Correlations Between Conformational Parameters in β-D-Furanoside Fragments Derived from a Statistical Survey of Crystal Structures of Nucleic Acid Constituents Full Description of Nucleoside Molecular Geometries in Terms of Four Parameters

3. Interpretation of vicinal proton-proton coupling constants by a generalized Karplus relation. Conformational analysis of the exocyclic C4′-C5′ bond in nucleosides and nucleotides: Preliminary Communication

4. in Topics in Stereochemistry, Vol. 10, ed. by and Wiley Interscience, New York (1978).

5. Conformations of proline

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