## Abstract Unambiguous and complete assignments of ^1^H and ^13^C NMR chemical shifts for three structurally complex labadane diterpenoids isolated from __Leonotis ocymifolia__ (leonotin, leonotinin and nepetaefolin) and six other related compounds (hispanolone, 7α‐ and 7β‐hispanols, marrubiin, vi
Structural and spectral assignment of a new diterpenoid isolated from Ballota undulata and a complete 1H and 13C NMR data assignment for three other structurally related compounds
✍ Scribed by Ahmed A. Hussein; María L. Jimeno; Benjamín Rodríguez
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 110 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2050
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✦ Synopsis
Abstract
The structure of 3β‐hydroxyballotinone, a new labdane diterpenoid isolated from Ballota undulata, has been established by NMR spectroscopic studies. In addition, complete and unambiguous assignments of the ^1^H and ^13^C NMR spectra of three other already known labdanes (ballotinone, ballonigrin and ballonigrinone) isolated from the same source have been achieved. The assignments are based on 2D shift‐correlated ^1^H^1^H COSY, ^1^H^13^C gHSQC [^1^J(C,H)] and ^1^H^13^C gHMBC [^n^J(C,H) (n = 2 and 3)], and NOE experiments. Copyright © 2007 John Wiley & Sons, Ltd.
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