✍ Scribed by Appell, Michael ;Krunic, Aleksej ;Choi, Tony Jeen ;Santhana Mariappan, S. V. ;Dunn III, William J. ;Reith, Maarten E. A.
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
NMR spectra of quinidine (I), hydroquinidine (II), and their respective acetyl derivatives (III and IV) were compared. The chemical shifts of some protons in I differed from those of their counterparts in II. These values were concentration dependent in I and II; they were similar in III and IV but
## Abstract The effect of thioamide substitution on the conformational stability of an azaglycine‐containing peptide, For‐AzaGly‐NH~2~ (**1**), was investigated for the sake of finding possible applications by using __ab initio__ and DFT methods. As model compounds, For‐[ΨCSNH]‐AzaGly‐NH~2~ (**2**)
The x-ray molecular structures of five chiral phosphoramidates derived from N-phosphorylated nitrogen mustard were determined and the molecular parameters are discussed. The value of the torsion angle of the O=P-N-H function which determines the packing of the molecules was found to determine also t
The long-standing issue of the conformational change of myo-inositol hexakisphosphoric acid (H 12 inhp), commonly called phytic acid, was resolved by low-temperature pH\* studies and NMR spectroscopy. Lowtemperature experiments on phytic acid, in a suitable mixed solvent and in the appropriate pH\*