Conformational studies of N‐acetyl‐N′‐methylamide derivatives of α‐aminobutyric acid, norvaline, and valine. I. Preferred conformations in solution as studied by 1H‐nmr spectroscopy
- 1 June 1988
- journal article
- research article
- Published by Wiley in Biopolymers
- Vol. 27 (6) , 969-984
- https://doi.org/10.1002/bip.360270607
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Side-chain torsional energies, conformer populations, and other tests of an improved conformational energy program for peptides: ECEPP83International Journal of Peptide and Protein Research, 1984
- A solvent effect on the side‐chain conformation of phenylalanine derivatives and phenylalanine residuces in dipeptidesBiopolymers, 1978
- Long range 13C1H spin-spin coupling constants in amino acids. Conformational applicationsJournal of Magnetic Resonance (1969), 1975
- Conformational energy map of a dipeptide unit in relation to infrared and nuclear magnetic resonance dataBiopolymers, 1971
- Studies on the conformation of amino acids. IX. Conformations of butyl, seryl, threonyl, cysteinyl, and valyl residues in a dipeptide unitBiopolymers, 1971
- Nuclear magnetic resonance study of some α-amino acids—II. Rotational isomerismSpectrochimica Acta, 1964
- A New Method of Forming Peptide BondsJournal of the American Chemical Society, 1955
- Near Infrared Spectra of Compounds with Two Peptide Bonds and the Configuration of a Polypeptide Chain. IV.Journal of the American Chemical Society, 1954
- Near Infrared Spectra of Compounds with Two Peptide Bonds and the Configuration of a Polypeptide Chain. IIIJournal of the American Chemical Society, 1953
- Near Infrared Spectra of Compounds with Two Peptide Bonds and the Configuration of a Polypeptide ChainJournal of the American Chemical Society, 1951