## Abstract The isolation and structure elucidation of a novel dimeric alkaloid, griffithine, from the leafy shoots of __Sophora griffithii__ Stock (Papilionaceae) is described. The alkaloid possesses a 12‐membered ring system formed by the linking of C‐10 and C‐10′ of the alkaloid with the N‐1 and
Structure elucidation of the oligosaccharide calonyctin A by the concerted use of 1D and 2D NMR techniques
✍ Scribed by Guy Serratrice; Raphaël Pastor; You-Chuan Hu
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 543 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The chemical structure of a plant growth substance, calonyctin A, was determined by NMR spectroscopy. The ^13^C and ^1^H spectral assignments were obtained using a combination of DEPT, heteronuclear chemical shift correlation, ^1^H–^1^H COSY, ^1^H–^1^H NOESY and inverse long‐range ^1^H–^13^C correlation. Calonyctin A was found to be a mixture of two homologous glycosides, each containing four rhamnoses and two aglycones. The configuration of the rhamnoses and the structural linkage between the six molecular fragments are reported.
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