## Abstract Three prenylflavanones, sigmoidins A, B and C, were studied using one‐ and two‐dimensional NMR techniques. The interpretation of these spectra led to the definitive assignments of all carbon and hydrogen chemical shifts.
2-Dimethoxyphosphoryl-1,3-dithiane: A comparison of NMR studies for 1H, 13C and 31P nuclei by one- and two-dimensional NMR techniques
✍ Scribed by Michael Engelhardt; Gerhard Hägele; Marian Mikolajczyk; Piotr Balczewski; Detlef Wendisch
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 403 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
2-Dimethoxyphosphoryl-l,3-dithiane was obtained by the reaction of 2-ddoro-1,3&thia~~e with trimethyl phosphite. Studies at 200,360 and 400 MHz using 'H, 13C and " P nuclei and lDand 2D NMR techniques are described. Long-range coupling constants were extracted by iterative treatment of [ A B ] , C D m spin systems. A rigid dithiane structure with axial phosphorus is consistent with the NMR results. Analogous dithianes and solid-state structures are discussed. 'H NMR STUDIES An appropriate description of the -CH,-CH,--CH,-unit in 1,3-dithianes such as 1-3 with a rigid Q W Scheme 1. Equatorial conformer of 1.
📜 SIMILAR VOLUMES
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
The 1H and 13C NMR spectra of 2-phenyl-3H-naphtho [2,1-b][1,4]oxazin-3-one, 2-p-methoxyphenylnaphtho [1,2-d]oxazole and 2-phenylnaphtho[1,2-d]oxazole were totally assigned using a combination of one-and two-dimensional NMR techniques. In addition to correlation of the proton signals by a COSY spectr
## Abstract A metabolite extracted from maize culture was identified as cyclonerodiol. Its ^1^H and ^13^C NMR spectra have been fully analysed, and some literature assignments have been reversed.
Total assignment of "C and 'H NMR spectra of the new compounds 1-cyano-and 1-phenyl-substituted 3,fdimethyl-2-thiatricycl0[3.2.l.l~~~]nonane 2,Z-dioxide was achieved using the concerted application of two-dimensional homonuclear and heteronuclear chemical shift correlations. This unequivocal structu
## Abstract The syntheses, ^1^H, ^13^C and ^31^P NMR chemical shifts and ^13^C‐^31^P coupling constants of 2‐aryloxy/cyclicamino‐2,3‐dihydro ‐3‐ (4‐methylphenyl) ‐1__H__ ‐ naphth [1,2__‐e__] [1,3,2]oxazaphosphorine 2‐oxides/sulphides and the ^13^C NMR data for 4‐substituted ‐ dinaphtho [2,1 ‐__d__: