## 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–
✦ LIBER ✦
Structure elucidation of a spirostanol glycoside from Asparagus officinalis fruits by concerted use of two-dimensional NMR techniques
✍ Scribed by G. Pant; M. S. Panwar; D. S. Negi; M. S. M. Rawat; Gareth A. Morris; R. I. G. Thompson
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 453 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Complete ''C and 'H assignments for the oligosaccharide segment of a novel spirostanol glycoside were derived, and structural proof obtained, using a combination of DEPT, heteronuclear chemical shift correlation, homonuclear relayed coherence transfer, absolute value COSY, phase-sensitive double quantum filtered COSY, NOESY, INEPT and protondetected long-range heteronuclear shift correlation via multiple quantum coherence.
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