Identification of structure and study of configuration of reaction products of endo-dicyclopentadiene with phenols by the1H and13C NMR method
✍ Scribed by V. P. Lezina; A. U. Stepanyants; A. S. Murakhovskaya; V. R. Melikyan; L. L. Vasil'eva; K. I. Zimina
- Book ID
- 112438923
- Publisher
- Springer
- Year
- 1974
- Tongue
- English
- Weight
- 211 KB
- Volume
- 23
- Category
- Article
- ISSN
- 1573-9171
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The carbon–carbon connectivity of terreinol, a new metabolite isolated from __Aspergillus terreus__, and its previous ^13^C assignments were confirmed by a two‐dimensional INADEQUATE experiment using a few milligrams of the compound with natural ^13^C abundance. The carbon–carbon correl
## Abstract The ^13^C and ^1^H NMR spectra of a series of methiodides of mono‐ and di‐C‐methyl derivatives of 1‐methyl‐4‐phenyl‐4‐piperidinols are reported and chemical shift data analysed in terms of configurations and conformations of isomeric sets. Results demondtrate the value of quaternary sal