13C nuclear magnetic resonance spectral and conformational analysis of naturally occurring tetrahydrofuran lignans
- 15 February 1979
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 57 (4), 441-443
- https://doi.org/10.1139/v79-071
Abstract
The 13C nmr spectra of the naturally occurring stereoisomers of the tetrahydrofuran lignans were recorded and the signals assigned. Based on these assignments, on the observed sensitivity of the benzylic carbon shifts to the orientation of the aryl groups, and on the comparison with previously reported 1H nmr data, the most probable conformations for the mentioned stereoisomers are suggested.Keywords
This publication has 3 references indexed in Scilit:
- Neolignans of Virola surinamensisPhytochemistry, 1978
- Studies in the indole series. VII. Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. XL. Carbon-13 nuclear magnetic resonance analysis of vobasine-like indole alkaloidsThe Journal of Organic Chemistry, 1976
- 13C NMR spectroscopy of neolignansPhytochemistry, 1976