## Abstract The complete assignment of the proton and carbon NMR spectra for seven sequiterpene alcohols isolated from the heartwood oil of __Neocallitropsis pancheri__, namely, α, β‐ and γ‐eudesmol, carissone, guaiol, bulnesol and elemol, was achieved using the concerted application of one‐and two
Two-dimensional nuclear magnetic resonance of sesquiterpenes. 4—Application to complete assignment of 1H and 13C NMR spectra of some aromadendrane derivatives
✍ Scribed by Robert Faure; Armand R. P. Ramanoelina; Olivier Rakotonirainy; Jean-Pierre Bianchini; Emile M. Gaydou
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 238 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The total assignment of the ^1^H and ^13^C NMR spectra of five aromadendrane derivatives, (+)‐aromadendrene (1), (−)‐alloaromadendrene (2), (+)‐ledene (3), (−)‐dehydroaromadendrane (4), (−)‐globulol (5) and (+)‐viridiflorol (6) has been performed. The ^13^C spectral assignment of globulol was achieved from DEPT and double quantum coherence measurements. The concerted application of ^1^H^1^H homonuclear and ^1^H^13^C heteronuclear two‐dimensional chemical shift correlations provided other ^13^C and all ^1^H chemical shifts. Moreover, the ^1^H assignment for compounds 13 was reexamined from the high‐field analysis of proton‐proton coupling constants.
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