Review: Contributions of NMR spectroscopy to the study of hydrogen bonds in serine protease active sites
β Scribed by William W. Bachovchin
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 331 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.951
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Splittings, 6,, were observed for each carbon atom, C,, of chalcone in spectra obtained from coaxial 5 and 10 mm NMR sample tubes containing solutions equimolar in the concentration of the ketone and of TFA or TFA-d as hydrogen-bond donors, respectively. It was found that a linear expression, S,A,+x
## Abstract The ^1^H, ^13^C and ^15^N NMR studies have shown that the __E__ and __Z__ isomers of pyrroleβ2βcarbaldehyde oxime adopt preferable conformation with the __syn__ orientation of the oxime group with respect to the pyrrole ring. The __syn__ conformation of __E__ and __Z__ isomers of pyrrol