NMR spectroscopic determination of preferred conformations of quinidine and hydroquinidine
β Scribed by Yehuda Yanuka; Shimona Yosselson Superstine; Edward Superstine
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 486 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
β¦ Synopsis
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 not concentration dependent. The implications of these findings and the correlation of the NMR data with the preferred conformations are discussed.
π SIMILAR VOLUMES
## Abstract A relaxation method was applied to quinidine (1) where crossβrelaxations (Ο~ij~) were obtained by ^1^H selective and biselective __T__~1~ measurements and correlation times for molecular reorientation (Ο~c~) were evaluated from the frequency dependence of the nonβselective __T__~1.~ The
The 2OOMHz 'H NMR spectra of pilocarpine, pilocarpine.HC1 and isopilocarpine.HC1 have been studied. Evidence is presented for the preferred conformations of the compounds in aqueous solution, with the methylimidazolyl moiety antiperiplanar with respect to the a-carbon of the butanolide ring.
## Abstract Hydroxyiridals β monocyclic triterpenoids β are found abundantly in sword lilies. They feature a homofarnesyl side chain that is hydroxylated at one of the allylic methylene groups, which gives rise to a chiral carbon atom. The absolute configuration of six hydroxyiridals from different