## Abstract When an isoalloxazine derivative (**1**) was reduced (**2**) its ^13^C‐NMR. resonances were all shifted upfield and the largest shifts were observed for C (4a), C(6) and C(8) but downfield shifts for C(2), C(4) and C(10a). The results and their biochemical implications are shortly discu
13C-NMR. Study on Isoalloxazine and Alloxazine Derivatives
✍ Scribed by Hans J. Grande; Robert Gast; Cees G. Van Schagen; Willem J. H. Van Berkel; Franz Müller
- Book ID
- 102857839
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 715 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A series of isoalloxazine and alloxazine derivatives have been investigated by ^13^C‐NMR. The synthesis of selectively ^13^C‐enriched derivatives made it possible to assign unambiguously the signals due to the quaternary carbon atoms at position 4, 4a and 10a of the isoalloxazine ring system. The assignment of the other resonances was ensured by the use of selectively deuteriated and chemically modified compounds as well as by decoupling techniques. The assignments differ in part from those published by Breitmaier & Voelter [2] on FMN and FAD. The solvent dependence of the resonances has been studied in dioxan/water mixtures. The experimental data are compared with published MO calculations and discussed.
📜 SIMILAR VOLUMES
## Abstract Assignment of all ^13^C chemical shifts of perezone (1) and some derivatives was possible using time averaged 25·15 MHz spectra with the aid of proton noise modulated and CW decoupling. Rapid interconversion of tautomeric forms of 2,5‐dihydroxy‐1,4‐benzoquinones is deduced from the ^13^