Excluding hyperconjugation from the Z conformational preference and investigating its origin: formic acid and beyond-Reference-Cited by-同舟云学术

Excluding hyperconjugation from the Z conformational preference and investigating its origin: formic acid and beyond

Published:2015 Issue:40 Volume:17 Page:26946-26954
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Ferro-Costas David¹²³⁴⁵,Mosquera Ricardo A.¹²³⁴⁵

Affiliation:

1. Departamento de Química Física

2. Universidade de Vigo

3. Facultade de Química

4. 36310 Vigo

5. Spain

Abstract

A scheme indicating that the preference for the Z conformer in proteins is chemically equivalent to that of amides. Other compounds, such as carboxylic acids, also exhibit the same conformational trend.

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CP/C5CP03805G

Reference50 articles.

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2. A. J. Kirby , The Anomeric Effect and Related Stereoelectronic Effects at Oxygen, Springer-Verlag, Berlin, 1983

3. E. Juaristi and G.Cuevas, The Anomeric Effect, CRC Press, Boca Ratón, Florida, 1995

4. E. L. Eliel , N. L.Allinger, S. J.Angyal and G. A.Morrison, Conformational Analysis, American Chemical Society, Washington, 1981

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