Joshi, Balawant S. ; Wunderlich, John K. ; William Pelletier, S. (1987) 13C Nuclear magnetic resonance spectroscopy in the elucidation of structures of diterpenoid alkaloids Canadian Journal of Chemistry / Revue Canadienne de Chimie, 65 (1). pp. 99-103. ISSN 0008-4042
Full text not available from this repository.
Official URL: http://www.nrcresearchpress.com/doi/abs/10.1139/v8...
Related URL: http://dx.doi.org/10.1139/v87-016
Abstract
13C Nuclear magnetic resonance spectroscopy is an exceptionally useful tool for the structure determination of diterpenoid alkaloids. A detailed study of the 1H and 13C nmr spectra of aconitine and 3-deoxyaconitine has permitted definite assignments to all the carbon atoms of the molecule. Chemical shift revisions have been suggested for certain carbon atoms of the C19-diterpenoid alkaloids. Chemical examination of Aconitumcolumbianum Nutt. ssp. columbianum, A. forrestii Stapf, Delphiniumtatsienense Franch., and D. vestitum Wall, resulted in the isolation of several new C19-diterpenoid alkaloids. The structure derivation of those alkaloids was based mainly on 13C nmr spectroscopic evidence.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to NRC Research Press. |
| ID Code: | 86883 |
| Deposited On: | 13 Mar 2012 14:57 |
| Last Modified: | 13 Mar 2012 14:57 |
Repository Staff Only: item control page
