## Abstract Three prenylflavanones, sigmoidins A, B and C, were studied using oneโ and twoโdimensional NMR techniques. The interpretation of these spectra led to the definitive assignments of all carbon and hydrogen chemical shifts.
13C NMR assignments of brassinosteroids by two-dimensional techniques
โ Scribed by Tetsu Ando; Masakazu Aburatani; Nozomu Koseki; Seiichi Asakawa; Takehito Mouri; Hiroshi Abe
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 481 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
Abstract
^1^H NMR spectra of eight naturally occurring brassinosteroids, plant hormones with a steroid skeleton, and five synthetic analogues were analysed by COSY and longโrange COSY measurements. Based on the ^1^H resonances, the ^13^C signals were assigned by a combination of C๏ฃฟH COSY and longโrange C๏ฃฟH COSY spectra detecting ^13^C nuclei, or by HMQC and HMBC spectra detecting ^1^H nuclei. Although the steroids showed complex ^1^H signals around 1โ2 ppm, the resonances for the two angular methyl groups and the other methyl groups in the sideโchain could be assigned unambiguously and used as a reference point for the other assignments. Strong correlation peaks between the methyl protons and carbons connected with the protons through two or three bonds were observed in the longโrange C๏ฃฟH COSY or the HMBC spectra. These spectra provide valuable information for assigning the ^13^C NMR resonances of this class of compounds.
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