Application of two-dimensional NMR spectroscopy to the complete analysis of the 1H and 13C NMR spectra of d-biotin in aqueous solution
✍ Scribed by Mitsuhiko Ikura; Kunio Hikichi
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 846 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^1^H and ^13^C NMR spectra of d‐biotin were observed at 400 and 100 MHz, respectively. Various types of two‐dimensional NMR spectroscopy were performed to assign the spectra. The previous assignment of ^13^C NMR spectrum of d‐biotin reported by Bradbury and Johnson was modified, and the dihedral angles between the CH bonds of the ring were determined. The populations of the conformers produced by internal rotation around the C‐2C‐δ bond were estimated.
📜 SIMILAR VOLUMES
COSY and NOESY spectra (400 MHz) have been used to complete the assignment of the 'H NMR spectra of 1and 3-nitrobenzo[e]pyrene. Both compounds show strong bay region nuclear Overhauser enhancement and significant coupling across bay regions. Both compounds also exhibit extensive long-range couplings
The total assignment of the 13C and the ' H NMR spectra of four derivatives of 1,3diaza-2,4-diboranaphthalene has been performed. The interpretation of the spectra was achieved from the concerted application of direct and long-range heteronuclear chemical shift correlation and homonuclear COSY two-d
## Abstract Following earlier studies on the development of one‐ and two‐dimensional NMR methods based on selection of coherences via maximum‐quantum pathways and using inverse ^1^H detection, a pulse sequence is now described for analogous direct heteronuclear detection for use in laboratories whi