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
β¦ LIBER β¦
A study of the structure and stereochemistry of corydaine and corpaine by means of the intramolecular nuclear Overhauser effect
β Scribed by D. A. Fesenko; M. E. Perel'son
- Book ID
- 112375558
- Publisher
- Springer
- Year
- 1971
- Tongue
- English
- Weight
- 148 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0009-3130
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Determination of the stereochemistry of
β
A. Liguori; R. OttanΓ ; G. Romeo; E. Rotondo; G. Sindona; N. Uccella
π
Article
π
1988
π
John Wiley and Sons
π
English
β 508 KB
Formations, analysis of cyanine dyes by
β
M. Yu. Kornilov; A. V. Turov; V. V. Kurdyukov; M. A. Kudinova; A. I. Tolmachev
π
Article
π
1989
π
Springer
π
English
β 372 KB
Proof of the position of the methoxy gro
β
M. R. Yagudaev; V. M. Malikov; S. Yu. Yunusov
π
Article
π
1973
π
Springer
π
English
β 145 KB
Mechanism of the intramolecular 1H nucle
β
T.Phil Pitner; Roderich Walter; Jerry D. Glickson
π
Article
π
1976
π
Elsevier Science
π
English
β 327 KB
Nuclear Overhauser effect, a unique meth
β
Woods, Marion C.; Chiang, Hung-Che.; Nakadaira, Yasuhiro.; Nakanishi, Koji.
π
Article
π
1968
π
American Chemical Society
π
English
β 276 KB
One- and two-dimensional nuclear overhau
β
A. Marsura; C. Luu-Duc; R. Nardin
π
Article
π
1985
π
John Wiley and Sons
π
English
β 540 KB
The study of 5-f~ctionalized 2-imidazolines by 'β¬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