A theoretical and experimental 1 H NMR spectroscopy study of the stereoelectronic interactions that rule the conformational energies of alanine and valine methyl ester-Reference-Cited by-同舟云学术

A theoretical and experimental 1 H NMR spectroscopy study of the stereoelectronic interactions that rule the conformational energies of alanine and valine methyl ester

Published:2013-07-30 Issue:10 Volume:26 Page:849-857
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Cormanich Rodrigo A.¹,Ducati Lucas C.²,Tormena Cláudio F.¹,Rittner Roberto¹

Affiliation:

1. Chemistry Institute; University of Campinas; P.O. Box 6154 13083-970 Campinas Brazil

2. Chemistry Institute; University of São Paulo; P. O. Box 26077 05508-900 São Paulo Brazil

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3180/fullpdf

Reference54 articles.

1. Are hydrogen bonds responsible for glycine conformational preferences?

2. The lack of intramolecular hydrogen bonding and the side chain effect in alanine conformers

3. A theoretical investigation of the dictating forces in small amino acid conformational preferences: The case of glycine, sarcosine and N,N-dimethylglycine

4. Conformers of gaseous glycine

5. Glycine conformational analysis

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