Conventional one-dimensional NMR methods and two-dimensional shift-correlated NMR experiments (COSY, HMQC, HMBC) were used for 1 H and 13 C chemical shift assignments of two naphthoquinone dimers tectol and tecomaquinone I isolated from Lippia sidoides.
Total assignment of the 1H and 13C NMR spectra of casimiroedine and its peracetylated derivative
β Scribed by William F. Reynolds; Raul G. Enriquez; Gil A. Magos; Dino Gnecco
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 51 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
The rare alkaloid casimiroedine and its peracetylated derivative both show complex 1 H and 13 C spectra with almost all signals doubled owing to slow rotation about the amide bond. Nevertheless, it is possible, using 2D NMR methods, to assign fully the 1 H and 13 C spectra of the major and minor conformational isomers for each compound.
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