After correlation of the majority of signals by COSY and one-bond heteronuclear correlation, the complete assignment of the 'H and I3C NMR spectra of the macrolide antibiotic venturicidin A required the application of long-range CH coupling information. This was accessible by the COLOC-S and selecti
New bitter saponins from the bark of Colubrina elliptica: 1H and 13C assignments by 2D NMR spectroscopy
✍ Scribed by Winston F. Tinto; William F. Reynolds; Compton E. Seaforth; Shaliza Mohammed; Anderson Maxwell
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 362 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Three new bitter saponins, designated mabioside A, B and C, were isolated from the bark of Colubrina elliptica and were determined to be 3‐O‐[α‐JL‐rhamnopyranosy]‐(1 → 6)‐β‐D‐glucopyranosyl‐15‐O‐[β‐D‐ glucopyranosyl] mabiogenin, 3‐O‐[α‐L‐rhamnopyranosy]‐(1 → 6)‐[β‐D‐glucopyranosyl‐(1 → 2)]‐β‐D‐glucopyranosyl}mabiogenin and 3‐O‐[α‐L‐rhamnopyranosyl‐(1 → 6)‐β‐D‐glucopyranosyl] mabiogenin, respectively. The structures were elucidated by using a combination of 2D NMR techniques (H‐H COSY, H‐H DQF‐COSY, RCT‐COSY, C‐H COSY, FLOCK, NOESY).
📜 SIMILAR VOLUMES
Three known bisabolane hydrocarbons, a-trans -bergamotene, sesquiphellandrene and zingiberene, were isolated from the aerial parts of Alpinia densibracteata . Their 1H and 13C NMR spectra were completely assigned by using a combination of 13C DEPT and 2D-NMR experiments (1H-1H COSY, single-bond 13C-