𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Nuclear Overhauser effect, a unique method of defining the relative stereochemistry and conformation of taxane derivatives

✍ Scribed by Woods, Marion C.; Chiang, Hung-Che.; Nakadaira, Yasuhiro.; Nakanishi, Koji.

Book ID
126801547
Publisher
American Chemical Society
Year
1968
Tongue
English
Weight
276 KB
Volume
90
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Determination of the stereochemistry of
Determination of the stereochemistry of isoxazolidinium salts by nuclear Overhauser effect difference spectroscopy
✍ A. Liguori; R. OttanΓ ; G. Romeo; E. Rotondo; G. Sindona; N. Uccella πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 508 KB

The configurations of some isoxazolidinium salts have been determined by nuclear Overhauser effect difference spectroscopy (NOEDS). The stereochemical findings give a good explanation of the different reactivities experienced in the five-membered ring-opening process as a function of the steric requ

One- and two-dimensional nuclear overhau
One- and two-dimensional nuclear overhauser effect. Investigation of the stereochemistry of 5-functionalized 2-imidazolines
✍ A. Marsura; C. Luu-Duc; R. Nardin πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 English βš– 540 KB

The study of 5-f~ctionalized 2-imidazolines by '€I NMR, l -D NOE and 2-D NOE is reported. The application of these methods con6rms the relative configurations and conformations of the compounds. In particular, NOE effects and related crystallographic data are in good agreement with the proposed angu